Modified helicases

ABSTRACT

The invention relates to modified helicases with reduced unbinding from polynucleotides. The helicases can be used to control the movement of polynucleotides and are particularly useful for sequencing polynucleotides.

FIELD OF THE INVENTION

The invention relates to modified helicases with reduced unbinding frompolynucleotides. The helicases can be used to control the movement ofpolynucleotides and are particularly useful for sequencingpolynucleotides.

BACKGROUND OF THE INVENTION

There is currently a need for rapid and cheap polynucleotide (e.g. DNAor RNA) sequencing and identification technologies across a wide rangeof applications. Existing technologies are slow and expensive mainlybecause they rely on amplification techniques to produce large volumesof polynucleotide and require a high quantity of specialist fluorescentchemicals for signal detection.

Transmembrane pores (nanopores) have great potential as direct,electrical biosensors for polymers and a variety of small molecules. Inparticular, recent focus has been given to nanopores as a potential DNAsequencing technology.

When a potential is applied across a nanopore, there is a change in thecurrent flow when an analyte, such as a nucleotide, resides transientlyin the barrel for a certain period of time. Nanopore detection of thenucleotide gives a current change of known signature and duration. Inthe strand sequencing” method, a single polynucleotide strand is passedthrough the pore and the identity of the nucleotides are derived. Strandsequencing can involve the use of a nucleotide handling protein, such asa helicase, to control the movement of the polynucleotide through thepore.

SUMMARY OF THE INVENTION

Helicases are enzymes that are capable of binding to and controlling themovement of polynucleotides. Several helicases, including Hel308helicases, have a polynucleotide binding domain which in at least oneconformational state has an opening through which the polynucleotide canbind or unbind from the helicase. This allows the helicase to disengagefrom a polynucleotide, even if the helicase is not positioned at an endof the polynucleotide.

The inventors have surprisingly demonstrated that the ability of ahelicase to control the movement of a polynucleotide can be improved byreducing the size of the opening through which the polynucleotideunbinds. In particular, the helicase's ability to control the movementof a polynucleotide can be improved by closing the opening. Inaccordance with the invention, the size of the opening is reduced or theopening is closed by connecting at least two parts of the helicase.

This result is surprising because a reduction in the size of the openingor a closing of the opening does not prevent the helicase from bindingto a polynucleotide. Once a helicase modified in accordance with theinvention has bound to a polynucleotide, it is capable of controllingthe movement of most of, if not all of, the polynucleotide withoutunbinding or disengaging. In particular, the inventors have surprisinglydemonstrated that helicases modified in accordance with the inventionwill strongly bind to a long polynucleotide, such as a polynucleotidecomprising 400 nucleotides or more, and will control the movement ofmost of, if not all of, the polynucleotide. This allows the effectivecontrol of the movement of the polynucleotide, especially during StrandSequencing.

The inventors have surprisingly demonstrated that the ability of aHel308 helicase to control the movement of a polynucleotide can beimproved by introducing one or more cysteine residues and/or one or morenon-natural amino acids at specific positions. Irrespective of whetheror not the introduced residues are connected, the modified Hel308helicase is capable of controlling the movement of most of, if not allof, a polynucleotide without unbinding or disengaging.

Accordingly, the invention provides a helicase formed from one or moremonomers and comprising a polynucleotide binding domain which comprisesin at least one conformational state an opening through which apolynucleotide can unbind from the helicase, wherein the helicase ismodified such that two or more parts on the same monomer of the helicaseare connected to reduce the size of the opening and wherein the helicaseretains its ability to control the movement of the polynucleotide.

The invention also provides:

-   -   a Hel308 helicase in which one or more cysteine residues and/or        one or more non-natural amino acids have been introduced at one        or more of the positions which correspond to D272, N273, D274,        G281, E284, E285, E287, S288, T289, G290, E291, D293, T294,        N300, R303, K304, N314, S315, N316, H317, R318, K319, L320,        E322, R326, N328, S615, K717, Y720, N721 and S724 in Hel308 Mbu        (SEQ ID NO: 10), wherein the helicase retains its ability to        control the movement of a polynucleotide;    -   a construct comprising a helicase of the invention and an        additional polynucleotide binding moiety, wherein the helicase        is attached to the polynucleotide binding moiety and the        construct has the ability to control the movement of a        polynucleotide;    -   a method of controlling the movement of a polynucleotide,        comprising contacting the polynucleotide with a helicase of the        invention or a construct of the invention and thereby        controlling the movement of the polynucleotide;    -   method of characterising a target polynucleotide, comprising (a)        contacting the target polynucleotide with a transmembrane pore        and a helicase of the invention or a construct of the invention        such that the helicase or the construct controls the movement of        the target polynucleotide through the pore and (b) taking one or        more measurements as the polynucleotide moves with respect to        the pore wherein the measurements are indicative of one or more        characteristics of the target polynucleotide and thereby        characterising the target polynucleotide;    -   a method of forming a sensor for characterising a target        polynucleotide, comprising forming a complex between (a) a pore        and (b) a helicase of the invention or a construct of the        invention and thereby forming a sensor for characterising the        target polynucleotide;    -   a sensor for characterising a target polynucleotide, comprising        a complex between (a) a pore and (b) a helicase of the invention        or a construct of the invention;    -   use of a helicase of the invention or a construct of the        invention to control the movement of a target polynucleotide        through a pore;    -   a kit for characterising a target polynucleotide comprising (a)        a pore and (b) a helicase of the invention or a construct of the        invention;    -   an apparatus for characterising target polynucleotides in a        sample, comprising (a) a plurality of pores and (b) a plurality        of helicases of the invention or a plurality of constructs of        the invention;    -   a method of producing a helicase of the invention,        comprising (a) providing a helicase formed from one or more        monomers and comprising a polynucleotide binding domain which        comprises an opening through which a polynucleotide can unbind        from the helicase and (b) modifying the helicase such that two        or more parts on the same monomer of the helicase are connected        to reduce the size of the opening and thereby producing a        helicase of the invention;    -   a method of producing a modified Hel308 helicase of the        invention, comprising (a) providing a Hel308 helicase and (b)        introducing one or more cysteine residues and/or one or more        non-natural amino acids at one or more of the positions which        correspond to D272, N273, D274, G281, E284, E285, E287, S288,        T289, G290, E291, D293, T294, N300, R303, K304, N314, S315,        N316, H317, R318, K319, L320, E322, R326, N328, 5615, K717,        Y720, N721 and S724 in Hel308 Mbu (SEQ ID NO: 10) and thereby        producing a modified Hel308 helicase of the invention; and    -   a method of producing a construct of the invention, comprising        attaching a helicase of the invention to an additional        polynucleotide binding moiety and thereby producing a construct        of the invention.

DESCRIPTION OF THE FIGURES

FIG. 1 shows a coomassie stained, 7.5% Tris-HCl gel (loaded with Laemmliloading buffer) of the Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 reactionmixture (SEQ ID NO: 10 with mutations E284C/S615C connected by abismaleimidePEG3 linker). Lane X shows an appropriate protein ladder(the mass unit markers are shown on the left of the gel). Lanes a-ccontain 2 μL, 5 μL or 10 μL of approximately 2.5 μM Hel308Mbu(E284C/S615C) monomer (SEQ ID NO: 10 with mutations E284C/S615C).Lanes d-f contain 2 μL, 5 μL or 10 μL of approximately 2.5 μM Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker, i.e. a helicase inwhich the opening has been closed), it was clear from the gel that thereaction to attach the bismaleimidePEG3 linker went to nearly 100%yield. Arrow 1 corresponds to Hel308 Mbu (E284C/S615C) monomer (SEQ IDNO: 10 with mutations E284C/S615C) and arrow 2 corresponds to Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker, i.e. a helicase inwhich the opening has been closed).

FIG. 2 shows a coomassie stained 7.5% Tris-HCl gel of the Hel308 Mbu(E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutations E284C/S615Cconnected by a bismaleimide peptide linker (maleimide-propyl-SRDFWRS(SEQ ID NO: 109)-(1,2-diaminoethane)-propyl-maleimide)) reactionmixture. Lane X shows an appropriate protein ladder (the mass unitmarkers are shown on the left of the gel). Lane A contains 5 μL ofapproximately 10 μM Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO:10 with the mutations E284C/S615C connected by a bismaleimidePEG3linker) as a reference. The upper band (labelled 2) corresponds toHel308 Mbu(E284C/S615C)-bismaleimidePEG3 and the lower band (labelled 1)to Hel308 Mbu (E284C/S615C) (SEQ ID NO: 10 with the mutationsE284C/S615C). Lane B contains 5 μL of approximately 10 μM Hel308 Mbu(E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutations E284C/S615Cconnected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide), it wasclear from the gel that the reaction to attach the mal-pep-mal linkerdid not go to completion as a band for the Hel308 Mbu(E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutations E284C/S615Cconnected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide) (upperband) and the Hel308 Mbu (E284C/S615C) (SEQ ID NO: 10 with the mutationsE284C/S615C) (lower band) are observed. Lane C contains Hel308 Mbu(E284C/S615C) (SEQ ID NO: 10 with the mutations E284C/S615C).

FIG. 3 shows a fluorescence assay used to compare the enzymeprocessivity of two Hel308 Mbu helicases in which the opening has beenclosed (Hel308 Mbu(E284C/S615C)-bismaleimidePEG11 (SEQ ID NO: 10 withmutations E284C/S615C connected by a bismaleimidePEG11 linker) andHel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker)) to that of theHel308 Mbu monomer (SEQ ID NO: 10). A custom fluorescent substrate wasused to assay the ability of the helicase to displace hybridised dsDNA.The fluorescent substrate (50 nM final) has a 3′ ssDNA overhang, and 80and 33 base-pair sections of hybridised dsDNA (section A, SEQ ID NO:110, labelled 1). The major bottom “template” strand is hybridised to an80 nt “blocker” strand (SEQ ID NO: 111, labelled 2), adjacent to its 3′overhang, and a 33 nt fluorescent probe (labelled 3), labelled at its 5′and 3′ ends with carboxyfluorescein (FAM, labelled 4) and black-holequencher (BHQ-1, labelled 5) bases (SEQ ID NO: 112), respectively. Whenhybridised, the FAM is distant from the BHQ-1 and the substrate isessentially fluorescent. In the presence of ATP (1 mM) and MgCl₂ (10mM), the helicase (labelled 6, 10 nM) binds to the substrate's 3′overhang (SEQ ID NO: 110), moves along the lower strand, and begins todisplace the 80 nt blocker strand (SEQ ID NO: 111), as shown in sectionB. If processive, the helicase displaces the fluorescent probe too(section C, SEQ ID NO: 112, labelled with a carboxyfluorescein (FAM) atits 5′ end a black-hole quencher (BHQ-1) at its 3′ end). The fluorescentprobe is designed in such a way that its 5′ and 3′ ends areself-complementary and thus form a kinetically-stable hairpin oncedisplaced, preventing the probe from re-annealing to the template strand(section D). Upon formation of the hairpin product, the FAM is broughtinto the vicinity of the BHQ-1 and its fluorescence is quenched. Aprocessive enzyme, capable of displacing the 80 mer “blocker” (SEQ IDNO: 111) and fluorescent (SEQ ID NO: 112, labelled with acarboxyfluorescein (FAM) at its 5′ end a black-hole quencher (BHQ-1) atits 3′ end) strands will therefore lead to a decrease in fluorescenceover time. However, if the enzyme has a processivity of less than 80 ntit would be unable to displace the fluorescent strand (SEQ ID NO: 112,labelled with a carboxyfluorescein (FAM) at its 5′ end a black-holequencher (BHQ-1) at its 3′ end) and, therefore, the “blocker” strand(SEQ ID NO: 111) would reanneal to the major bottom strand (section E).

FIG. 4 shows additional custom fluorescent substrates which were alsoused for control purposes. The substrate used as a negative control wasidentical to that of the one described in FIG. 3 but lacking the 3′overhang (section A, (SEQ ID NO's: 111 (labelled 2 in figure), 112(Strand labelled 3 in figure, labelled with a carboxyfluorescein (FAM,labelled 4 in figure) at its 5′ end a black-hole quencher (BHQ-1,labelled 5 in figure) at its 3′ end) and 113 labelled 7 in figure)). Asimilar substrate to that described in FIG. 3 but lacking the 80 basepair section (SEQ ID NO's: 112 (strand labelled 3 in figure, labelledwith a carboxyfluorescein (FAM labelled 4 in figure) at its 5′ end ablack-hole quencher (BHQ-1, labelled 5 in figure) at its 3′ end) and 114labelled 8 in figure), was used as a positive control for active, butnot necessarily processive, helicases (section B).

FIG. 5 shows a graph (y-axis label=Normalised fluorescence (arbitraryvalues), x-axis label=time (min)) of the time-dependent fluorescencechanges upon testing Hel308 Mbu, Hel308Mbu(E284C/S615C)-bismaleimidePEG11 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG11 linker) and Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker) against theprocessivity substrate shown in FIG. 3 in buffered solution (400 mMNaCl, 10 mM Hepes pH 8.0, 1 mM ATP, 10 mM MgCl₂, 50 nM fluorescentsubstrate DNA (SEQ ID NOs: 110, 111 and 112 (labelled with acarboxyfluorescein (FAM) at its 5′ end a black-hole quencher (BHQ-1) atits 3′ end). The data points marked with a black diamond correspond to abuffer blank, the white square data points correspond to Hel308 Mbumonomer (SEQ ID NO: 10), the black cross data points correspond toHel308 Mbu(E284C/S615C)-bismaleimidePEG11 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG11 linker) and the whitecircle data points correspond to Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker). The decrease influorescence exhibited by Hel308 Mbu(E284C/S615C)-bismaleimidePEG1 (SEQID NO: 10 with mutations E284C/S615C connected by a bismaleimidePEG11linker) and Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 withmutations E284C/S615C connected by a bismaleimidePEG3 linker), denotethe increased processivity of these complexes as compared to Hel308 Mbumonomer (SEQ ID NO: 10).

FIG. 6 shows a graph (y-axis label=Normalised fluorescence (arbitraryvalues), x-axis label=time (min)) of the time-dependent fluorescencechanges upon testing Hel308 Mbu (SEQ ID NO: 10), Hel308Mbu(E284C/S615C)-bismaleimidePEG11 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG11 linker) and Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker) against the positivecontrol processivity substrate (shown in FIG. 4 section B, SEQ ID NOs:112 (labelled with a carboxyfluorescein (FAM) at its 5′ end a black-holequencher (BHQ-1) at its 3′ end) and 60) in buffered solution (400 mMNaCl, 10 mM Hepes pH 8.0, 1 mV ATP, 10 mM MgCl₂, 50 nM fluorescentsubstrate DNA (SEQ ID NOs: 112 (labelled with a carboxyfluorescein (FAM)at its 5′ end a black-hole quencher (BHQ-1) at its 3′ end) and 114)).The data points marked with a black diamond correspond to a bufferblank, the white square data points correspond to Hel308 Mbu monomer(SEQ ID NO: 10), the black cross data points correspond to Hel308Mbu(E284C/S615C)-bismaleimidePEG11 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG11 linker) and the whitecircle data points correspond to Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker). This positivecontrol demonstrated that all complexes were indeed active, as denotedby a fluorescence decrease for all samples.

FIG. 7 shows a schematic of enzyme controlled translocation of apolynucleotide through a nanopore in a membrane, where the enzymecontrols the movement of the polynucleotide against the force of theapplied field. The schematic shows the example of a 3′ to 5′ enzyme(labelled A), where the capture of a polynucleotide in the pore by the5′ end leads to the enzyme controlling the movement of thepolynucleotide (the polynucleotide sequences used in example 4 are SEQID NO: 115 (labelled B in FIG. 7), SEQ ID NO:116 (labelled C in FIG. 7)and SEQ ID NO: 117 (labelled D in FIG. 7)) against the force of theapplied field. During DNA capture the hybridised strands are unzipped.Arrow 1 denotes the direction of DNA movement through the nanopore, thewhite arrow 2 denotes the direction of enzyme movement along the DNA andarrow 3 denotes the direction of the applied field. As long as theenzyme does not dissociate from the DNA the enzyme will pull the DNA outof the pore until it is finally ejected on the cis side of the membrane.

FIG. 8 shows a schematic of enzyme controlled translocation of apolynucleotide through a nanopore in a membrane, where the enzymecontrols the movement of the polynucleotide in the same direction as theforce of the applied field. The schematic shows the example of a 3′ to5′ enzyme (labelled A), where the capture of a polynucleotide in thepore by the 3′ end leads to the enzyme controlling the movement of thepolynucleotide with the force of the applied field. Arrow 1 denotes thedirection of the DNA movement through the nanopore, the white arrow 2denotes the direction of enzyme movement along DNA and arrow 3 denotesthe direction of the applied field. As long as the enzyme does notdissociate from the DNA the enzyme will feed the DNA through the poreuntil it is finally ejected on the trans side of the membrane.

FIG. 9 shows the DNA substrate design used in Example 4. The 900mersense strand (SEQ ID NO: 115) is labelled A, the anti-sense strand whichis minus the 4 base-pair leader (SEQ ID NO: 116) is labelled B and theprimer (SEQ ID NO: 117) is labelled C. The primer has a 3′ cholesteroltag which is labelled D.

FIG. 10 shows example current traces observed when a helicase controlsthe translocation of DNA (+140 mV, 400 mM NaCl, 100 mM Hepes pH 8.0, 10mM potassium ferrocyanide, 10 mM potassium ferricyanide, 0.1 nM 900merDNA (SEQ ID NO: 115, 116 and 117 (which at the 3′ end of the sequencehas six iSp18 spacers attached to two thymine residues and a 3′cholesterol TEG)), 1 mM ATP, 1 mM MgCl₂) through an MspA nanopore(MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 with mutationsG75S/G77S/L88N/Q126R) using Hel308 Mbu monomer (200 nM, SEQ ID NO: 10).The top electrical trace (y-axis label=current (pA), x-axis label=time(min)) shows the open pore current (˜120 pA) dropping to a DNA level(20-50 pA) when DNA is captured under the force of the applied potential(+140 mV). DNA with enzyme attached results in a long block that showsstepwise changes in current as the enzyme moves the DNA through thepore. The upper trace shows a sequence of 8 separate helicase-controlledDNA movements marked A-H. All of the helicase-controlled DNA movementsin this section of trace are being moved through the nanopore againstthe field by the enzyme (DNA captured 5′ down) (see FIG. 7 for details).Below are enlargements of the last section of 4 of thehelicase-controlled DNA movements as the DNA exits the nanopore. Of the8 helicase-controlled DNA movements in this section, only 1 (H) ends inthe characteristic long polyT level that indicates that the enzyme hasreached the end of the DNA and moved the 50T 5′-leader of the DNAsubstrate through the pore (labelled with a *). In the full run withHel308Mbu (SEQ ID NO: 10) it was found that ˜30% of thehelicase-controlled DNA movements end at the polyT (n=19helicase-controlled DNA movements in this experiment).

FIG. 11 shows example current traces observed when a helicase controlsthe translocation of DNA (+140 mV, 400 mM NaCl, 100 mM Hepes pH 8.0, 10mM potassium ferrocyanide, 10 mM potassium ferricyanide, 0.05 nM 900merDNA (SEQ ID NO: 115, 116 and 117 (which at the 3′ end of the sequencehas six iSp18 spacers attached to two thymine residues and a 3′cholesterol TEG)), 2 mM ATP, 2 mM MgCl₂) through an MspA nanopore(MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 with mutationsG75S/G77S/L88N/Q126R) using the Hel308 Mbu(E284C/S615C)-bismaleimidePEG3(10 nM, SEQ ID NO: 10 with mutations E284C/S615C connected by abismaleimidePEG3 linker). The top electrical trace (y-axis label=current(pA), x-axis label=time (min)) shows the open pore current (˜115 pA)dropping to a DNA level (15-40 pA) when DNA is captured under the forceof the applied potential (+140 mV). DNA with enzyme attached results ina long block that shows stepwise changes in current as the enzyme movesthe DNA through the pore. The upper trace shows a sequence of 8 separatehelicase-controlled DNA movements marked A-H. All thehelicase-controlled DNA movements in this section of trace are beingmoved through the nanopore against the field by the enzyme (DNA captured5′ down) (see FIG. 7 for details). Below are enlargements of the lastsection of 4 of the helicase-controlled DNA movements as the DNA exitsthe nanopore. Of the 8 helicase-controlled DNA movements in thissection, every one ends in the characteristic long polyT level thatindicates that the enzyme has reached the end of the DNA and moved the50T 5′-leader of the DNA substrate through the pore (labelled with a *).In the full run with Hel308 Mbu (E284C/S615C)-bismaleimidePEG3 (SEQ IDNO: 10 with mutations E284C/S615C connected by a bismaleimidePEG3linker) it was found that 85% of the helicase-controlled DNA movementsagainst the field (5′ down) end at the polyT (n=27 helicase-controlledDNA movements in this experiment).

FIG. 12 shows example current traces observed when a helicase controlsthe translocation of DNA (+140 mV, 400 mM NaCl, 100 mM Hepes pH 8.0, 10mM potassium ferrocyanide, 10 mM potassium ferricyanide, 0.05 nM 900merDNA (SEQ ID NO: 115, 116 and 117 (which at the 3′ end of the sequencehas six iSp18 spacers attached to two thymine residues and a 3′cholesterol TEG)), 2 mM ATP, 2 mM MgCl₂) through an MspA nanopore(MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 with mutationsG75S/G77S/L88N/Q126R) using the Hel308 Mbu(E284C/S615C)-bismaleimidePEG3(10 nM, SEQ ID NO: 10 with mutations E284C/S615C connected by abismaleimidePEG3 linker). The top electrical trace (y-axis label=current(pA), x-axis label=time (min)) shows the open pore current (˜120 pA)dropping to a DNA level (15-40 pA) when DNA is captured under the forceof the applied potential (+140 mV). DNA with enzyme attached results ina long block that shows stepwise changes in current as the enzyme movesthe DNA through the pore. The upper trace shows a sequence of 4 separatehelicase-controlled DNA movements marked A-D. All thehelicase-controlled DNA movements in this section of trace are beingmoved through the nanopore with the field by the enzyme (DNA captured 3′down) (see FIG. 8 for details). Below are enlargements of the lastsection of the helicase-controlled DNA movements as the DNA exits thenanopore. 3′ down DNA shows a characteristically different signature to5′ down DNA, with a different current to sequence relationship, anddifferent variance. Of the 4 helicase-controlled DNA movements in thissection, every one ends in the characteristic long polyT level thatindicates that the enzyme has reached the end of the DNA and moved the50T 5′-leader of the DNA substrate through the pore (labelled with a *).In the full run with Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ IDNO: 10 with mutations E284C/S615C connected by a bismaleimidePEG3linker) it was found that ˜87% of the helicase-controlled DNA movementswith the field (3′ down) end at the polyT (n=15 helicase-controlled DNAmovements in this experiment).

FIG. 13 shows example current traces (y-axis=current (pA), x-axis=time(s) for upper and lower traces) observed when a helicase controls thetranslocation of DNA (+120 mV, (625 mM KCl, 100 mM Hepes, 75 mMPotassium Ferrocyanide (II), 25 mM Potassium ferricyanide (III), pH 8,0.5 nM DNA (SEQ ID NO: 127 attached at its 3′ end to four iSpC3 spacers,the last of which is attached to the 5′ end of SEQ ID NO: 128), 1 mMATP, 10 mM MgCl₂) through an MspA nanopore (MS(B1-G75S/G77S/L88N/Q126R)8MspA (SEQ ID NO: 2 with mutations G75S/G77S/L88N/Q126R) using the Hel308Mbu (E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutationsE284C/S615C connected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS (SEQ ID NO:109)-(1,2-diaminoethane)-propyl-maleimide)). The top electrical traceshows the open pore current (˜400 pA) dropping to a DNA level (250-220pA) when DNA is captured under the force of the applied potential (+120mV). DNA with enzyme attached results in a long block that showsstepwise changes in current as the enzyme moves the DNA through thepore. The lower trace is a zoomed in region of the upper trace.

FIG. 14 shows a coomassie stained 7.5% Tris-HCl gel of the TrwCCba-N691C/Q346C-mal-PEG11-mal (SEQ ID NO: 126 with the mutationsN691C/Q346C connected by a bismaleimide polyethylene glycol linker)reaction mixture. The lane on the right of the gel (labelled M) shows anappropriate protein ladder (the mass unit markers are shown on the rightof the gel). Lane 1 contains 5 μL of approximately 10 μM TrwCCba-D657C/R339C alone (SEQ ID NO: 126 with mutation D657C/R339C) as areference. Lane 2 contains 5 μL of approximately 10 μM TrwCCba-N691C/Q346C-bismaleimidePEG11 (SEQ ID NO: 126 with the mutationsN691C/Q346C connected by a bismaleimide PEG11 linker). As indicated inlane 2, the upper band corresponds to the dimeric enzyme species(labelled A), the middle band corresponds to the closed complex(labelled B) TraI-Cba-N691C/Q346C-bidmaleimidePEG11 (SEQ ID NO: 126 withthe mutations N691C/Q346C connected by a bismaleimide PEG11 linker). Itwas clear from the gel that the reaction to attach the mal-PEG11-mallinker did not go to completion as a band for unmodified startingmaterial (labelled C) TrwC Cba-N691C/Q346C (SEQ ID NO: 126 with themutations N691C/Q346C) was observed.

FIG. 15 shows a fluorescence assay for testing the rate of turnover ofdsDNA molecules (min⁻¹ enzyme⁻¹). A custom fluorescent substrate wasused to assay the ability of the helicase (a) to displace hybridiseddsDNA. 1) The fluorescent substrate strand (50 nM final, SEQ ID NO: 151and 152) has both a 3′ and 5′ ssDNA overhang. The upper strand (b) has acarboxyfluorescein base (c) near the 5′ end (the carboxyfluorescein isattached to a modified thymine at position 6 in SEQ ID NO: 151), and thehybridised complement (d) has a black-hole quencher (BHQ-1) base (e)near the 3′ end (the black-hole quencher is attached to a modifiedthymine at position 81 in SEQ ID NO: 152). When hybridised, thefluorescence from the fluorescein is quenched by the local BHQ-1, andthe substrate is essentially non-fluorescent. 1 μM of a capture strand(f, SEQ ID NO: 153) that is part-complementary to the lower strand ofthe fluorescent substrate is included in the assay. 2) In the presenceof ATP (1 mM) and MgCl₂ (10 mM), helicase (10 nM) added to the substratebinds to the 3′ tail of the fluorescent substrate, moves along the upperstrand, and displaces the complementary strand (d) as shown. 3) Once thecomplementary strand with BHQ-1 is fully displaced the fluorescein onthe major strand fluoresces. 4) Displaced lower strand (d)preferentially anneals to an excess of capture strand (f) to preventre-annealing of initial substrate and loss of fluorescence.

FIG. 16 shows dsDNA turnover (enzyme⁻¹min⁻¹) in buffer (400 mM KCl, 100mM Hepes pH 8.0, 1 mV ATP, 10 mM MgCl₂, 50 nM fluorescent substrate DNA(SEQ ID NOs: 151 and 152), 1 μM capture DNA (SEQ ID NO: 153)) for anumber of helicases (Hel308 Mbu (labelled 1, SEQ ID NO: 10), Hel308Mbu-E284C (labelled 2, SEQ ID NO: 10 with the mutation E284C), Hel308Mbu-E284C/C301A (labelled 3, SEQ ID NO: 10 with the mutationsE284C/C301A), Hel308 Mbu-E285C (labelled 4, SEQ ID NO: 10 with themutation E285C) and Hel308Mbu-S288C (labelled 5, SEQ ID NO: 10 with themutation S288C)). Hel308 Mbu-E284C (SEQ ID NO: 10 with the mutationE284C), Hel308 Mbu-E284C/C301A (SEQ ID NO: 10 with the mutationsE284C/C301A), Hel3081Mbu-E285C (SEQ ID NO: 10 with the mutation E285C)and Hel308 Mbu-S288C (SEQ ID NO: 10 with the mutation S288C) showedincreased rate of turnover of dsDNA molecules (min⁻¹enzyme⁻¹) whencompared to Hel308 Mbu (SEQ ID NO: 10).

FIG. 17 shows dsDNA turnover (enzyme⁻¹ min⁻¹) in buffer (400 mM KCl, 100mM Hepes pH 8.0, 1 mM ATP, 10 mM MgCl₂, 50 nM fluorescent substrate DNA(SEQ ID NOs: 151 and 152), 1 μM capture DNA (SEQ ID NO: 153)) for anumber of helicases (Hel308 Mbu (labelled 1, SEQ ID NO: 10), Hel308Mbu-E284C (labelled 2, SEQ ID NO: 10 with the mutation E284C) and Hel308Mbu-D274C (labelled 6, SEQ ID NO: 10 with the mutation D274C)). Hel308Mbu-E284C (SEQ ID NO: 10 with the mutation E284C) and Hel308 Mbu-D274C(SEQ ID NO: 10 with the mutations D274C) showed increased rate ofturnover of dsDNA molecules (min⁻¹enzyme⁻¹) when compared to Hel308 Mbu(SEQ ID NO: 10).

FIG. 18 shows a schematic of enzyme controlled translocation of apolynucleotide through a nanopore in a membrane, where the enzymecontrols the movement of the polynucleotide against the force of theapplied field. The schematic shows the example of a 3′ to 5′ enzyme(labelled A), where the capture of a polynucleotide (the polynucleotidesequences used in Example 9 are SEQ ID NO: 154 (labelled B in FIG. 18),SEQ ID NO: 155 (labelled C in FIG. 18) and SEQ ID NO: 156 (labelled D inFIG. 18) and SEQ ID NO: 117 (labelled E in FIG. 18)) in the pore by the5′ end leads to the enzyme controlling the movement of thepolynucleotide against the force of the applied field (the direction ofthe applied field is indicated by arrow 1). During DNA capture thehybridised strands are unzipped. Arrow 2 denotes the direction of DNAmovement through the nanopore and the arrow 3 denotes the direction ofenzyme movement along the DNA. As long as the enzyme does not dissociatefrom the DNA the enzyme will pull the DNA out of the pore until it isfinally ejected on the cis side of the membrane.

FIG. 19 shows an example current trace (y-axis=current (pA), x-axis=time(s)) observed when Hel308 Mbu (SEQ ID NO: 10) controls the translocationof DNA (+120 mV, (960 mM KCl, 25 mM potassium phosphate, 3 mM potassiumferrocyanide, 1 mM potassium ferricyanide pH 8.0, 10 mM MgCl₂ and 1 mMATP) 0.2 nM DNA ((SEQ ID NO: 154 attached at its 5′ end to fournitroindoles the last of which is attached to the 3′ end of SEQ ID NO:155), SEQ ID NO: 156 and SEQ ID NO: 117) through an MspA nanopore(MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 with mutationsG75S/G77S/L88N/Q126R). The electrical trace shows the open pore current(˜250 pA) dropping to a DNA level (˜50 pA) when DNA is captured underthe force of the applied potential (+120 mV). DNA with enzyme attachedresults in a long block that shows stepwise changes in current as theenzyme moves the DNA through the pore.

FIG. 20 shows example current traces (y-axis=current (pA), x-axis=time(s) for both traces) observed when Hel308 Mbu-E284C (SEQ ID NO: 10 withthe mutation E284C) controls the translocation of DNA (+120 mV, (960 mVKCl, 25 mM potassium phosphate, 3 mM potassium ferrocyanide, 1 mMpotassium ferricyanide pH 8.0, 10 mM MgCl₂ and 1 mM ATP) 0.2 nM DNA((SEQ ID NO: 154 attached at its 5′ end to four nitroindoles the last ofwhich is attached to the 3′ end of SEQ ID NO: 155), SEQ ID NO: 156 andSEQ ID NO: 117) through an MspA nanopore (MS(B1-G75S/G77S/L88N/Q126R)8MspA (SEQ ID NO: 2 with mutations G75S/G77S/L88N/Q126R). The upperelectrical trace shows the DNA level (˜35 pA) when DNA is captured underthe force of the applied potential (+120 mV). DNA with enzyme attachedresults in a long block that shows stepwise changes in current as theenzyme moves the DNA through the pore. The lower trace shows a zoomed inview of the helicase controlled DNA movement shown in the upper trace.

FIG. 21 shows example current traces (y-axis=current (pA), x-axis=time(s) for both traces) observed when Hel308 Mbu-S288C (SEQ ID NO: 10 withthe mutation S288C) controls the translocation of DNA (+120 mV, (960 mVKCl, 25 mM potassium phosphate, 3 mM potassium ferrocyanide, 1 mMpotassium ferricyanide pH 8.0, 10 mM MgCl₂ and 1 mM ATP) 0.2 nM DNA((SEQ ID NO: 154 attached at its 5′ end to four nitroindoles the last ofwhich is attached to the 3′ end of SEQ ID NO: 155), SEQ ID NO: 156 andSEQ ID NO: 117) through an MspA nanopore (MS(B1-G75S/G77S/L88N/Q126R)8MspA (SEQ ID NO: 2 with mutations G75S/G77S/L88N/Q126R). The upperelectrical trace shows the DNA level (˜40 pA) when DNA is captured underthe force of the applied potential (+120 mV). DNA with enzyme attachedresults in a long block that shows stepwise changes in current as theenzyme moves the DNA through the pore. The lower trace shows a zoomed inview of the helicase controlled DNA movement shown in the upper trace.

FIG. 22 shows example current traces (y-axis=current (pA), x-axis=time(s) for both traces) observed when Hel308 Mbu-E284Faz (SEQ ID NO: 10with the mutation E284Faz) controls the translocation of DNA (+120 mV,(960 mM KCl, 25 mM potassium phosphate, 3 mM potassium ferrocyanide, 1mM potassium ferricyanide pH 8.0, 10 mM MgCl₂ and 1 mM ATP) 0.2 nM DNA((SEQ ID NO: 154 attached at its 5′ end to four nitroindoles the last ofwhich is attached to the 3′ end of SEQ ID NO: 155), SEQ ID NO: 156 andSEQ ID NO: 117) through an MspA nanopore (MS(B1-G75S/G77S/L88N/Q126R)8MspA (SEQ ID NO: 2 with mutations G75S/G77S/L88N/Q126R). The upperelectrical trace shows the DNA level (˜50 pA) when DNA is captured underthe force of the applied potential (+120 mV). DNA with enzyme attachedresults in a long block that shows stepwise changes in current as theenzyme moves the DNA through the pore. The lower trace shows a zoomed inview of the helicase controlled DNA movement shown in the upper trace.

FIG. 23 shows example current traces (y-axis=current (pA), x-axis=time(s) for both traces) observed when heat treated Hel308 Mbu-E284Faz (SEQID NO: 10 with the mutation E284Faz, the enzyme was heated in 50 mM TrispH 8.0, 375 mM NaCl, 5% Glycerol buffer from 4° C. to 50° C. for 10 minsand then cooled to 4° C. in a BioRad PCR block) controls thetranslocation of DNA (+120 mV, (960 mM KCl, 25 mM potassium phosphate, 3mM potassium ferrocyanide, 1 mM potassium ferricyanide pH 8.0, 10 mMMgCl₂ and 1 mM ATP) 0.2 nM DNA ((SEQ ID NO: 154 attached at its 5′ endto four nitroindoles the last of which is attached to the 3′ end of SEQID NO: 155), SEQ ID NO: 156 and SEQ ID NO: 117) through an MspA nanopore(MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 with mutationsG75S/G77S/L88N/Q126R). The upper electrical trace shows the DNA level(˜50 pA) for a number of helicase controlled DNA movements (eachmovement is numbered 1-3) when DNA is captured under the force of theapplied potential (+120 mV). DNA with enzyme attached results in a longblock that shows stepwise changes in current as the enzyme moves the DNAthrough the pore. The lower trace shows a zoomed in view of the helicasecontrolled DNA movement labelled 1 in the upper trace.

DESCRIPTION OF THE SEQUENCE LISTING

SEQ ID NO: 1 shows the codon optimised polynucleotide sequence encodingthe MS-B1 mutant MspA monomer. This mutant lacks the signal sequence andincludes the following mutations: D90N, D91N, D93N, D118R, D134R andE139K.

SEQ ID NO: 2 shows the amino acid sequence of the mature form of theMS-B1 mutant of the MspA monomer. This mutant lacks the signal sequenceand includes the following mutations: D90N, D91N, D93N, D118R, D134R andE139K.

SEQ ID NO: 3 shows the polynucleotide sequence encoding one monomer ofα-hemolysin-E111N/K147N (α-HL-NN; Stoddart et al., PNAS, 2009; 106(19):7702-7707).

SEQ ID NO: 4 shows the amino acid sequence of one monomer of α-HL-NN.

SEQ ID NOs: 5 to 7 show the amino acid sequences of MspB, C and D.

SEQ ID NO: 8 shows the amino acid sequence of the Hel308 motif.

SEQ ID NO: 9 shows the amino acid sequence of the extended Hel308 motif.

SEQ ID NOs: 10 to 58 show the amino acid sequences of Hel308 helicasesin Table 1.

SEQ ID NO: 59 shows the RecD-like motif I.

SEQ ID NOs: 60 to 62 show the extended RecD-like motif I.

SEQ ID NO: 63 shows the ReD motif I.

SEQ ID NO: 64 shows a preferred RecD motif I, namely G-G-P-G-T-G-K-T.

SEQ ID NOs: 65 to 67 show the extended RecD motif I.

SEQ ID NO: 68 shows the RecD-like motif V.

SEQ ID NO: 69 shows the RecD motif V.

SEQ ID NOs: 70 to 77 show the MobF motif III.

SEQ ID NOs: 78 to 84 show the MobQ motif III.

SEQ ID NO: 85 shows the amino acid sequence of TraI Eco.

SEQ ID NO: 86 shows the RecD-like motif I of TraI Eco.

SEQ ID NO: 87 shows the RecD-like motif V of TraI Eco.

SEQ ID NO: 88 shows the MobF motif III of TraI Eco.

SEQ ID NO: 89 shows the XPD motif V.

SEQ ID NO: 90 shows XPD motif VI.

SEQ ID NO: 91 shows the amino acid sequence of XPD Mbu.

SEQ ID NO: 92 shows the XPD motif V of XPD Mbu.

SEQ ID NO: 93 shows XPD motif VI of XPD Mbu.

SEQ ID NO: 94 shows the amino acid sequence of a preferred HhH domain.

SEQ ID NO: 95 shows the amino acid sequence of the ssb from thebacteriophage RB69, which is encoded by the gp32 gene.

SEQ ID NO: 96 shows the amino acid sequence of the ssb from thebacteriophage T7, which is encoded by the gp2.5 gene.

SEQ ID NO: 97 shows the amino acid sequence of the UL42 processivityfactor from Herpes virus 1.

SEQ ID NO: 98 shows the amino acid sequence of subunit 1 of PCNA.

SEQ ID NO: 99 shows the amino acid sequence of subunit 2 of PCNA.

SEQ ID NO: 100 shows the amino acid sequence of subunit 3 of PCNA.

SEQ ID NO: 101 shows the amino acid sequence of Phi29 DNA polymerase.

SEQ ID NO: 102 shows the amino acid sequence (from 1 to 319) of the UL42processivity factor from the Herpes virus 1.

SEQ ID NO: 103 shows the amino acid sequence of the ssb from thebacteriophage RB69, i.e. SEQ ID NO: 95, with its C terminus deleted(gp32RB69CD).

SEQ ID NO: 104 shows the amino acid sequence (from 1 to 210) of the ssbfrom the bacteriophage T7 (gp2.5T7-R211Del). The full length protein isshown in SEQ ID NO: 96.

SEQ ID NO: 105 shows the amino acid sequence of the 5^(th) domain ofHel308 Hla.

SEQ ID NO: 106 shows the amino acid sequence of the 5^(th) domain ofHel308 Hvo.

SEQ ID NO: 107 shows the amino acid sequence of the (HhH)2 domain.

SEQ ID NO: 108 shows the amino acid sequence of the (HhH)2-(HhH)2domain.

SEQ ID NO: 109 shows the amino acid sequence of the peptide linker usedto form a helicase in which the opening has been closed.

SEQ ID NOs: 110 to 117 show polynucleotide sequences used in theExamples.

SEQ ID NO: 118 shows the amino acid sequence of the human mitochondrialSSB (HsmtSSB).

SEQ ID NO: 119 shows the amino acid sequence of the p5 protein fromPhi29 DNA polymerase.

SEQ ID NO: 120 shows the amino acid sequence of the wild-type SSB fromE. coli.

SEQ ID NO: 121 shows the amino acid sequence of the ssb from thebacteriophage T4, which is encoded by the gp32 gene.

SEQ ID NO: 122 shows the amino acid sequence of EcoSSB-CterAla.

SEQ ID NO: 123 shows the amino acid sequence of EcoSSB-CterNGGN.

SEQ ID NO: 124 shows the amino acid sequence of EcoSSB-Q152del.

SEQ ID NO: 125 shows the amino acid sequence of EcoSSB-G117del.

SEQ ID NO: 126 shows the amino acid sequence of TrwC Cba.

SEQ ID NO: 127 shows part of the polynucleotide sequence used in Example5. Attached to the 3′ end of this sequence are four iSpC3 spacers unitsthe last of which is attached to the 5′ end of SEQ ID NO: 128.

SEQ ID NO: 128 shows part of the polynucleotide sequence used in Example5. Attached to the 5′ end of this sequence are four iSpC3 spacers unitsthe last of which is attached to the 3′ end of SEQ ID NO: 127.

SEQ ID NO: 129 shows the amino acid sequence of Topoisomerase V Mka(Methanopyrus Kandleri).

SEQ ID NO: 130 shows the amino acid sequence of domains H-L ofTopoisomerase V Mka (Methanopyrus Kandleri).

SEQ ID NOs: 131 to 139 show some of the TraI sequences shown in Table 3.

SEQ ID NO: 140 shows the amino acid sequence of Mutant S (Escherichiacoli).

SEQ ID NO: 141 shows the amino acid sequence of Sso7d (Sufolobussolfataricus).

SEQ ID NO: 142 shows the amino acid sequence of Sso10b1 (Sulfolobussolfataricus P2).

SEQ ID NO: 143 shows the amino acid sequence of Sso10b2 (Sulfolobussolfataricus P2).

SEQ ID NO: 144 shows the amino acid sequence of Tryptophan repressor(Escherichia coli).

SEQ ID NO: 145 shows the amino acid sequence of Lambda repressor(Enterobacteria phage lambda).

SEQ ID NO: 146 shows the amino acid sequence of Cren7 (Histonecrenarchaea Cren7 Sso).

SEQ ID NO: 147 shows the amino acid sequence of human histone (Homosapiens).

SEQ ID NO: 148 shows the amino acid sequence of dsbA (Enterobacteriaphage T4).

SEQ ID NO: 149 shows the amino acid sequence of Rad51 (Homo sapiens).

SEQ ID NO: 150 shows the amino acid sequence of PCNA sliding clamp(Citromicrobium bathyomarinum JL354).

SEQ ID NO: 151 shows one of the sequences used in Example 7. Thissequence has a carboxyfluorescein attached to a modified thymine locatedat position 6.

SEQ ID NO: 152 shows one of the sequences used in Example 7. Thissequence has a black-hole quencher (BHQ-1) attached to a modifiedthymine at position 81.

SEQ ID NO: 153 shows one of the sequences used in Example 7.

SEQ ID NO: 154 shows one of the sequences used in Example 9. Thissequence is attached at its 5′ end by four nitroindoles to the 3′ end ofSEQ ID NO: 155.

SEQ ID NO: 155 shows one of the sequences used in Example 9. Thissequence is attached at its 3′ end by four nitroindoles to the 5′ end ofSEQ ID NO: 154.

SEQ ID NO: 156 shows one of the sequences used in Example 9.

DETAILED DESCRIPTION OF THE INVENTION

It is to be understood that different applications of the disclosedproducts and methods may be tailored to the specific needs in the art.It is also to be understood that the terminology used herein is for thepurpose of describing particular embodiments of the invention only, andis not intended to be limiting.

In addition as used in this specification and the appended claims, thesingular forms “a”, “an”, and “the” include plural referents unless thecontent clearly dictates otherwise. Thus, for example, reference to “ahelicase” includes “helicases”, reference to “an opening” includes twoor more such openings, reference to “a transmembrane protein pore”includes two or more such pores, and the like.

All publications, patents and patent applications cited herein, whethersupra or infra, are hereby incorporated by reference in their entirety.

Modified Helicases with Two or More Parts Connected

The present invention provides a modified helicase that is useful forcontrolling the movement of a polynucleotide. The modified helicase isbased on an unmodified helicase having one or more monomers. In otherwords, the helicase may be monomeric or oligomeric/multimeric. This isdiscussed in more detail below. The modified helicase is based on anunmodified helicase comprising a polynucleotide binding domain whichcomprises in at least one conformational state an opening through whicha polynucleotide can unbind from the helicase. In accordance with theinvention, the helicase is modified such that two or more parts on thesame monomer of the helicase are connected to reduce the size of theopening. The reduced size of the opening does not prevent the helicasefrom binding to a polynucleotide. For instance, the helicase may bind toa polynucleotide at one of its termini. The reduced size of the openingdecreases the ability of the polynucleotide to unbind or disengage fromthe helicase, particularly from internal nucleotides of thepolynucleotide. This is discussed in more detail below and allows themodified helicase to remain bound to the polynucleotide for longer. Themodified helicase has the ability to control the movement of apolynucleotide. The modified helicase is artificial or non-natural.

The ability of a helicase to bind to and unbind from a polynucleotidecan be determined using any method known in the art. Suitablebinding/unbinding assays include, but are not limited to, nativepolyacrylamide gel electrophoresis (PAGE), fluorescence anisotropy,calorimetry and Surface plasmon resonance (SPR, such as Biacore™). Theability of a helicase to unbind from a polynucleotide can of course bedetermined by measuring the time for which the helicase can control themovement of a polynucleotide. This may also be determined using anymethod known in the art. The ability of a helicase to control themovement of a polynucleotide is typically assayed in a nanopore system,such as the ones described below. The ability of a helicase to controlthe movement of a polynucleotide can be determined as described in theExamples.

A modified helicase of the invention is a useful tool for controllingthe movement of a polynucleotide during Strand Sequencing. A problemwhich occurs in sequencing polynucleotides, particularly those of 500nucleotides or more, is that the molecular motor which is controllingthe movement of the polynucleotide may disengage from thepolynucleotide. This allows the polynucleotide to be pulled through thepore rapidly and in an uncontrolled manner in the direction of theapplied field. A modified helicase of the invention is less likely tounbind or disengage from the polynucleotide being sequenced. Themodified helicase can provide increased read lengths of thepolynucleotide as they control the movement of the polynucleotidethrough a nanopore. The ability to move an entire polynucleotide througha nanopore under the control of a modified helicase of the inventionallows characteristics of the polynucleotide, such as its sequence, tobe estimated with improved accuracy and speed over known methods. Thisbecomes more important as strand lengths increase and molecular motorsare required with improved processivity. A modified helicase of theinvention is particularly effective in controlling the movement oftarget polynucleotides of 500 nucleotides or more, for example 1000nucleotides, 5000, 10000, 20000, 50000, 100000 or more.

A modified helicase of the invention is also a useful tool forisothermal polymerase chain reaction (PCR). In such methods, the strandsof double stranded DNA are typically first separated by a helicase ofthe invention and coated by single stranded DNA (ssDNA)-bindingproteins. In the second step, two sequence specific primers typicallyhybridise to each border of the DNA template. DNA polymerases may thenbe used to extend the primers annealed to the templates to produce adouble stranded DNA and the two newly synthesized DNA products may thenbe used as substrates by the helicases of the invention, entering thenext round of the reaction. Thus, a simultaneous chain reactiondevelops, resulting in exponential amplification of the selected targetsequence.

The modified helicase has the ability to control the movement of apolynucleotide. The ability of a helicase to control the movement of apolynucleotide can be assayed using any method known in the art. Forinstance, the helicase may be contacted with a polynucleotide and theposition of the polynucleotide may be determined using standard methods.The ability of a modified helicase to control the movement of apolynucleotide is typically assayed in a nanopore system, such as theones described below and, in particular, as described in the Examples.

A modified helicase of the invention may be isolated, substantiallyisolated, purified or substantially purified. A helicase is isolated orpurified if it is completely free of any other components, such aslipids, polynucleotides, pore monomers or other proteins. A helicase issubstantially isolated if it is mixed with carriers or diluents whichwill not interfere with its intended use. For instance, a helicase issubstantially isolated or substantially purified if it is present in aform that comprises less than 10%, less than 5%, less than 2% or lessthan 1% of other components, such as lipids, polynucleotides, poremonomers or other proteins.

A helicase for use in the invention comprises a polynucleotide bindingdomain. A polynucleotide binding domain is the part of the helicase thatis capable of binding to a polynucleotide. Polynucleotides are definedbelow. The ability of a domain to bind a polynucleotide can bedetermined using any method known in the art. The polynucleotide bindingdomains of known helicases have typically been identified in the art.The domain (with or without bound polynucleotide) may be identifiedusing protein modelling, x-ray diffraction measurement of the protein ina crystalline state (Rupp B (2009). Biomolecular Crystallography:Principles, Practice and Application to Structural Biology. New York:Garland Science.), nuclear magnetic resonance (NMR) spectroscopy of theprotein in solution (Mark Rance; Cavanagh, John; Wayne J. Fairbrother;Arthur W. Hunt III; Skelton, NNicholas J. (2007). Protein NMRspectroscopy: principles and practice (2nd ed.). Boston: AcademicPress.) or cryo-electron microscopy of the protein in a frozen-hydratedstate (van Heel M, Gowen B, Matadeen R, Orlova E V, Finn R, Pape T,Cohen D, Stark H, Schmidt R, Schatz M, Patwardhan A (2000).“Single-particle electron cryo-microscopy: towards atomic resolution.”.Q Rev Biophys. 33: 307-69. Structural information of proteins determinedby above mentioned methods are publicly available from the protein bank(PDB) database.

Protein modelling exploits the fact that protein structures are moreconserved than protein sequences amongst homologues. Hence, producingatomic resolution models of proteins is dependent upon theidentification of one or more protein structures that are likely toresemble the structure of the query sequence. In order to assess whethera suitable protein structure exists to use as a “template” to build aprotein model, a search is performed on the protein data bank (PDB)database. A protein structure is considered a suitable template if itshares a reasonable level of sequence identity with the query sequence.If such a template exists, then the template sequence is “aligned” withthe query sequence, i.e. residues in the query sequence are mapped ontothe template residues. The sequence alignment and template structure arethen used to produce a structural model of the query sequence. Hence,the quality of a protein model is dependent upon the quality of thesequence alignment and the template structure.

Proteins, such as helicases, are dynamic structures which are inconstant motion. The conformational space that a protein can explore hasbeen described by an energy landscape, in which different conformationsare populated based on their energies, and rates of interconversion aredependent on the energy barriers between states (Vinson, Science, 2009:324(5924): 197). Helicases can therefore exist in several conformationstates whether in isolation or controlling the movement of apolynucleotide. In at least one conformational state, the polynucleotidebinding domain of an unmodified helicase for use in the inventioncomprises an opening through which a polynucleotide can unbind from thehelicase. The opening may be present in all conformational states of thehelicase, but does not have to be. For instance, in all conformationalstates, the polynucleotide binding domain may comprise an openingthrough which a polynucleotide can unbind from the helicase.Alternatively, in one or more conformational states of the helicase, thepolynucleotide binding domain may comprise an opening through which apolynucleotide cannot unbind from the helicase because the opening istoo small. In one or more conformational states of the helicase, thepolynucleotide binding domain may not comprise an opening through whicha polynucleotide can unbind from the helicase.

The polynucleotide binding domain preferably comprises in at least oneconformational state an opening through which one or more internalnucleotides of the polynucleotide can unbind from the helicase. Aninternal nucleotide is a nucleotide which is not a terminal nucleotidein the polynucleotide. For example, it is not a 3′ terminal nucleotideor a 5′ terminal nucleotide. All nucleotides in a circularpolynucleotide are internal nucleotides. Reducing or preventing theunbinding from one or more internal nucleotides in accordance with theinvention is advantageous because it results in modified helicases thatare capable of binding to one terminus of a polynucleotide, controllingthe movement of most, if not all of, the polynucleotide and thenunbinding at the other terminus. Such helicases are particularly helpfulfor Strand Sequencing.

The ability of one or more internal nucleotide to unbind from thehelicase may be determined by carrying out a comparative assay. Forinstance, the ability of a helicase to unbind from a controlpolynucleotide A is compared with its ability to unbind from the samepolynucleotide but with a blocking group attached at the terminalnucleotides (polynucleotide B). The blocking group prevents anyunbinding at the terminal nucleotide of strand B, and thus allows onlyinternal unbinding of the helicase. Alternatively, the ability of ahelicase to unbind from a circular polynucleotide may be assayed.Unbinding may be assayed as described above.

The opening may be a groove, pocket or recess in the polynucleotidebinding domain.

The presence of an opening through which a polynucleotide can unbindfrom the helicase can be determined using any method known in the art.The presence of an opening can be determined by measuring the ability ofa helicase to unbind from a polynucleotide, and in particular frominternal nucleotides of the polynucleotide, as discussed in more detailabove. Openings in the polynucleotide domain can be identified usingprotein modelling, x-ray diffraction, NMR spectroscopy or cryo-electronmicroscopy as discussed above.

In accordance with the invention, the helicase is modified by connectingtwo or more parts on the same monomer of the helicase. If the helicaseis oligomeric or multimeric, the two or more parts cannot be ondifferent monomers. Any number of parts, such as 3, 4, 5 or more parts,may be connected. Preferred methods of connecting the two or more partsare discussed in more detail below.

The two or more parts can be located anywhere on the monomer as long asthey reduce the size of the opening when connected in accordance withthe invention. The two or more parts may be in the polynucleotide domainor the opening, but do not have to be. For instance, one, both or all ofthe two or more parts may be outside the polynucleotide binding domain,such as on different domain of the helicase. The maximum distancebetween the two or more parts is the circumference of the helicase.

The two or more parts are preferably spatially proximate. The two ormore parts are preferably less that 50 Angstroms (Å) apart, such as lessthan 40 Å apart, less than 30 Å apart, less than 25 Å apart, less than20 Å apart, less than 10 Å apart or less than 10 Å apart.

At least one of the two or more parts preferably forms part of theopening, is adjacent to the opening or is near the opening. It isstraightforward to identify parts of the opening, such as amino acidswithin the opening, as described above. Parts are adjacent to theopening if they are next to, but do not form part of the opening. Forinstance, an amino acid which is located next to an amino acid thatforms part of the opening, but which itself does not form part of theopening is adjacent to the opening. In the context of the invention,“next to” may mean next to in the amino acid sequence of the helicase ornext two in the three-dimensional structure of the helicase. Apart istypically near to the opening if it is less than 20 Å from an amino acidthat forms part of the opening, such as less than 15 Å, less than 10 Å,less than 5 Å or less than 2 Å apart from an amino acid that forms partof the opening. A part is typically near to the opening if it is within1, 2, 3, 4 or 5 amino acids of an amino acid that forms part of theopening in the amino acid sequence of the helicase. Such amino acids maybe identified as discussed above.

The two or more parts may be on opposite sides of the opening. The twoor more parts may be on the same side of the opening. In thisembodiment, the two or more parts of the helicase may be connected toform a loop, lid, constriction or flap that reduces the size of theopening.

The two or more parts are preferably on the surface of the monomer, i.e.on the surface of the helicase. It is straightforward to connect two ormore parts on the surface as described in more detail below. Surfaceparts may be determined using protein modelling, x-ray diffraction, NMRspectroscopy or cryo-electron microscopy as discussed above.

The modified helicase retains its ability to control the movement of apolynucleotide. This ability of the helicase is typically provided byits three dimensional structure that is typically provided by itsβ-strands and α-helices. The α-helices and β-strands are typicallyconnected by loop regions. In order to avoid affecting the ability ofthe helicase to control the movement of a polynucleotide, the two ormore parts are preferably loop regions of the monomer. The loop regionsof specific helicases can be identified using methods known in the art,such as protein modelling, x-ray diffraction, NMR spectroscopy orcryo-electron microscopy as discussed above.

For Hel308 helicases (SEQ ID NOs: 10, 13, 16, 19, 22, 25, 28, 29, 32,33, 34, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52,53, 54, 55 and 58), β-strands can only be found in the two RecA-likeengine domains (domains 1 and 2). These domains are responsible forcoupling the hydrolysis of the fuel nucleotide (normally ATP) withmovement. The important domains for ratcheting along a polynucleotideare domains 3 and 4, but above all domain 4. Interestingly, both ofdomains 3 and 4 comprise only α-helices. There is an important α-helixin domain 4 called the ratchet helix. As a result, in the Hel308embodiments of the invention, the two or more parts are preferably notin any of the α-helixes.

The size of the opening may be reduced to any degree as long as itreduces the unbinding of the polynucleotides from the helicase. This maybe determined as discussed above. Ways in which the size of the openingare reduced are discussed in more detail below.

The two or more parts are preferably connected to close the opening. Ifthe opening is closed, the polynucleotide cannot unbind from thehelicase through the opening. The helicase is more preferably modifiedsuch that it does not comprise the opening in any conformational state.If the opening is not present in any conformational state of thehelicase, the polynucleotide cannot unbind from the helicase through theopening. The helicase is most preferably modified such that it iscapable of forming a covalently-closed structure around thepolynucleotide. Once the covalently-closed structure is bound to apolynucleotide, for instance at one end of the polynucleotide, it iscapable of controlling the movement of the polynucleotide withoutunbinding until it reaches the other end.

Connection

The two or more parts may be connected in any way. The connection can betransient, for example non-covalent. Even transient connection willreduce the size of the opening and reduce unbinding of thepolynucleotide from the helicase through the opening.

The two or more parts are preferably connected by affinity molecules.Suitable affinity molecules are known in the art. The affinity moleculesare preferably (a) complementary polynucleotides (InternationalApplication No. PCT/GB10/000132 (published as WO 2010/086602), (b) anantibody or a fragment thereof and the complementary epitope(Biochemistry 6th Ed, W.H. Freeman and co (2007) pp 953-954), (c)peptide zippers (O'Shea et al., Science 254 (5031): 539-544), (d)capable of interacting by β-sheet augmentation (Remaut and WaksmanTrends Biochem. Sci. (2006) 31 436-444), (e) capable of hydrogenbonding, pi-stacking or forming a salt bridge, (f) rotaxanes (Xiang Maand He Tian Chem. Soc. Rev., 2010, 39, 70-80), (g) an aptamer and thecomplementary protein (James, W. in Encyclopedia of AnalyticalChemistry, R. A. Meyers (Ed.) pp. 4848-4871 John Wiley & Sons Ltd,Chichester, 2000) or (h) half-chelators (Hammerstein et al. J Biol Chem.2011 Apr. 22; 286(16): 14324-14334). For (e), hydrogen bonding occursbetween a proton bound to an electronegative atom and anotherelectronegative atom. Pi-stacking requires two aromatic rings that canstack together where the planes of the rings are parallel. Salt bridgesare between groups that can delocalize their electrons over severalatoms, e. g. between aspartate and arginine.

The two or more parts may be transiently connected by a hexa-his tag orNi-NTA. The two or more parts may also be modified such that theytransiently connect to each other.

The two or more parts are preferably permanently connected. In thecontext of the invention, a connection is permanent if is not brokenwhile the helicase is used or cannot be broken without intervention onthe part of the user, such as using reduction to open —S—S— bonds.

The two or more parts are preferably covalently-attached. The two ormore parts may be covalently attached using any method known in the art.

The two or more parts may be covalently attached via their naturallyoccurring amino acids, such as cysteines, threonines, serines,aspartates, asparagines, glutamates and glutamines. Naturally occurringamino acids may be modified to facilitate attachment. For instance, thenaturally occurring amino acids may be modified by acylation,phosphorylation, glycosylation or farnesylation. Other suitablemodifications are known in the art. Modifications to naturally occurringamino acids may be post-translation modifications. The two or more partsmay be attached via amino acids that have been introduced into theirsequences. Such amino acids are preferably introduced by substitution.The introduced amino acid may be cysteine or a non-natural amino acidthat facilitates attachment. Suitable non-natural amino acids include,but are not limited to, 4-azido-L-phenylalanine (Faz), any one of theamino acids numbered 1-71 included in FIG. 1 of Liu C. C. and Schultz P.G., Annu. Rev. Biochem., 2010, 79, 413-444 or any one of the amino acidslisted below. The introduced amino acids may be modified as discussedabove.

In a preferred embodiment, the two or more parts are connected usinglinkers. Linker molecules are discussed in more detail below. Onesuitable method of connection is cysteine linkage. This is discussed inmore detail below. The two or more parts are preferably connected usingone or more, such as two or three, linkers. The one or more linkers maybe designed to reduce the size of, or close, the opening as discussedabove. If one or more linkers are being used to close the opening asdiscussed above, at least a part of the one or more linkers ispreferably oriented such that it is not parallel to the polynucleotidewhen it is bound by the helicase. More preferably, all of the linkersare oriented in this manner. If one or more linkers are being used toclose the opening as discussed above, at least a part of the one or morelinkers preferably crosses the opening in an orientation that is notparallel to the polynucleotide when it bound by the helicase. Morepreferably, all of the linkers cross the opening in this manner. Inthese embodiments, at least a part of the one or more linkers may beperpendicular to the polynucleotide. Such orientations effectively closethe opening such that the polynucleotide cannot unbind from the helicasethrough the opening.

Each linker may have two or more functional ends, such as two, three orfour functional ends. Suitable configurations of ends in linkers arewell known in the art.

One or more ends of the one or more linkers are preferably covalentlyattached to the helicase. If one end is covalently attached, the one ormore linkers may transiently connect the two or more parts as discussedabove. If both or all ends are covalently attached, the one or morelinkers permanently connect the two or more parts.

At least one of the two or more parts is preferably modified tofacilitate the attachment of the one or more linkers. Any modificationmay be made. The linkers may be attached to one or more reactivecysteine residues, reactive lysine residues or non-natural amino acidsin the two or more parts. The non-natural amino acid may be any of thosediscussed above. The non-natural amino acid is preferably4-azido-L-phenylalanine (Faz). At least one amino acid in the two ormore parts is preferably substituted with cysteine or a non-naturalamino acid, such as Faz.

The one or more linkers are preferably amino acid sequences and/orchemical crosslinkers.

Suitable amino acid linkers, such as peptide linkers, are known in theart. The length, flexibility and hydrophilicity of the amino acid orpeptide linker are typically designed such that it reduces the size ofthe opening, but does not to disturb the functions of the helicase.Preferred flexible peptide linkers are stretches of 2 to 20, such as 4,6, 8, 10 or 16, serine and/or glycine amino acids. More preferredflexible linkers include (SG)₁, (SG)₂, (SG)₃, (SG)₄, (SG)₅, (SG)₈,(SG)₁₀, (SG)₁₅ or (SG)₂₀ wherein S is serine and G is glycine. Preferredrigid linkers are stretches of 2 to 30, such as 4, 6, 8, 16 or 24,proline amino acids. More preferred rigid linkers include (P)₁₂ whereinP is proline. The amino acid sequence of a linker preferably comprises apolynucleotide binding moiety. Such moieties and the advantagesassociated with their use are discussed below.

Suitable chemical crosslinkers are well-known in the art. Suitablechemical crosslinkers include, but are not limited to, those includingthe following functional groups: maleimide, active esters, succinimide,azide, alkyne (such as dibenzocyclooctynol (DIBO or DBCO), difluorocycloalkynes and linear alkynes), phosphine (such as those used intraceless and non-traceless Staudinger ligations), haloacetyl (such asiodoacetamide), phosgene type reagents, sulfonyl chloride reagents,isothiocyanates, acyl halides, hydrazines, disulphides, vinyl sulfones,aziridines and photoreactive reagents (such as aryl azides,diaziridines).

Reactions between amino acids and functional groups may be spontaneous,such as cysteine/maleimide, or may require external reagents, such asCu(I) for linking azide and linear alkynes.

Linkers can comprise any molecule that stretches across the distancerequired. Linkers can vary in length from one carbon (phosgene-typelinkers) to many Angstroms. Examples of linear molecules, include butare not limited to, are polyethyleneglycols (PEGs), polypeptides,polysaccharides, deoxyribonucleic acid (DNA), peptide nucleic acid(PNA), threose nucleic acid (TNA), glycerol nucleic acid (GNA),saturated and unsaturated hydrocarbons, polyamides. These linkers may beinert or reactive, in particular they may be chemically cleavable at adefined position, or may be themselves modified with a fluorophore orligand. The linker is preferably resistant to dithiothreitol (DTT).

Preferred crosslinkers include 2,5-dioxopyrrolidin-1-yl3-(pyridin-2-yldisulfanyl)propanoate, 2,5-dioxopyrrolidin-1-yl4-(pyridin-2-yldisulfanyl)butanoate and 2,5-dioxopyrrolidin-1-yl8-(pyridin-2-yldisulfanyl)octananoate, di-maleimide PEG 1k, di-maleimidePEG 3.4k, di-maleimide PEG 5k, di-maleimide PEG 10k,bis(maleimido)ethane (BMOE), bis-maleimidohexane (BMH),1,4-bis-maleimidobutane BNB), 1,4 bis-maleimidyl-2,3-dihydroxybutane(BMDB), BM[PEO]2 (1,8-bis-maleimidodiethyleneglycol), BM[PEO]3(1,11-bis-maleimidotriethylene glycol), tris[2-maleimidoethyl]amine(TMEA), DTME dithiobismaleimidoethane, bis-maleimide PEG3, bis-maleimidePEG11, DBCO-maleimide, DBCO-PEG4-maleimide, DBCO-PEG4-NH2,DBCO-PEG4-NHS, DBCO-NHS, DBCO-PEG-DBCO 2.8 kDa, DBCO-PEG-DBCO 4.0 kDa,DBCO-15 atoms-DBCO, DBCO-26 atoms-DBCO, DBCO-35 atoms-DBCO,DBCO-PEG4-S—S-PEG3-biotin, DBCO-S-S-PEG3-biotin, DBCO-S-S-PEG11-biotin,(succinimidyl 3-(2-pyridyldithio)propionate (SPDP) and maleimide-PEG(2kDa)-maleimide (ALPHA,OMEGA-BIS-MALEIMIDO POLY(ETHYLENE GLYCOL)). Themost preferred crosslinker ismaleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide as used inthe Examples.

The one or more linkers may be cleavable. This is discussed in moredetail below.

The two or more parts may be connected using two different linkers thatare specific for each other. One of the linkers is attached to one partand the other is attached to another part. The linkers should react toform a modified helicase of the invention. The two or more parts may beconnected using the hybridization linkers described in InternationalApplication No. PCT/GB10/000132 (published as WO 2010/086602). Inparticular, the two or more parts may be connected using two or morelinkers each comprising a hybridizable region and a group capable offorming a covalent bond. The hybridizable regions in the linkershybridize and link the two or more parts. The linked parts are thencoupled via the formation of covalent bonds between the groups. Any ofthe specific linkers disclosed in International Application No.PCT/GB10/000132 (published as WO 2010/086602) may be used in accordancewith the invention.

The two or more parts may be modified and then attached using a chemicalcrosslinker that is specific for the two modifications. Any of thecrosslinkers discussed above may be used.

The linkers may be labeled. Suitable labels include, but are not limitedto, fluorescent molecules (such as Cy3 or AlexaFluor®555),radioisotopes, e.g. ¹²⁵I, ³⁵S, enzymes, antibodies, antigens,polynucleotides and ligands such as biotin. Such labels allow the amountof linker to be quantified. The label could also be a cleavablepurification tag, such as biotin, or a specific sequence to show up inan identification method, such as a peptide that is not present in theprotein itself, but that is released by trypsin digestion.

A preferred method of connecting the two or more parts is via cysteinelinkage. This can be mediated by a bi-functional chemical crosslinker orby an amino acid linker with a terminal presented cysteine residue.Linkage can occur via natural cysteines in the helicase. Alternatively,cysteines can be introduced into the two or more parts of the helicase.If the two or more parts are connected via cysteine linkage, the one ormore cysteines have preferably been introduced to the two or more partsby substitution.

The length, reactivity, specificity, rigidity and solubility of anybi-functional linker may be designed to ensure that the size of theopening is reduced sufficiently and the function of the helicase isretained. Suitable linkers include bismaleimide crosslinkers, such as1,4-bis(maleimido)butane (BMB) or bis(maleimido)hexane. One draw back ofbi-functional linkers is the requirement of the helicase to contain nofurther surface accessible cysteine residues if attachment at specificsites is preferred, as binding of the bi-functional linker to surfaceaccessible cysteine residues may be difficult to control and may affectsubstrate binding or activity. If the helicase does contain severalaccessible cysteine residues, modification of the helicase may berequired to remove them while ensuring the modifications do not affectthe folding or activity of the helicase. This is discussed inInternational Application No. PCT/GB10/000133 (published as WO2010/086603). The reactivity of cysteine residues may be enhanced bymodification of the adjacent residues, for example on a peptide linker.For instance, the basic groups of flanking arginine, histidine or lysineresidues will change the pKa of the cysteines thiol group to that of themore reactive S group. The reactivity of cysteine residues may beprotected by thiol protective groups such as5,5′-dithiobis-(2-nitrobenzoic acid) (dTNB). These may be reacted withone or more cysteine residues of the helicase before a linker isattached. Selective deprotection of surface accessible cysteines may bepossible using reducing reagents immobilized on beads (for exampleimmobilized tris(2-carboxyethyl) phosphine, TCEP). Cysteine linkage ofthe two or more parts is discussed in more detail below.

Another preferred method of attaching the two or more parts is via4-azido-L-phenylalanine (Faz) linkage. This can be mediated by abi-functional chemical linker or by a polypeptide linker with a terminalpresented Faz residue. The one or more Faz residues have preferably beenintroduced to the helicase by substitution. Faz linkage of two or morehelicases is discussed in more detail below.

Helicase

Any helicase formed of one or monomers and comprising a polynucleotidebinding domain which comprises in at least one conformational state anopening through which a polynucleotide can unbind from the helicase maymodified in accordance with the invention. Helicases are often known astranslocases and the two terms may be used interchangeably.

Suitable helicases are well-known in the art (M. E. Fairman-Williams etal., Curr. Opin. Struct Biol., 2010, 20 (3), 313-324, T. M. Lohman etal., Nature Reviews Molecular Cell Biology, 2008, 9, 391-401).

The helicase is preferably a member of superfamily 1 or superfamily 2.The helicase is more preferably a member of one of the followingfamilies: Pif1-like, Upf1-like, UvrD/Rep, Ski-like, Rad3/XPD,NS3/NPH-II, DEAD, DEAH/RHA, RecG-like, REcQ-like, T1R-like, Swi/Snf-likeand Rig-I-like. The first three of those families are in superfamily 1and the second ten families are in superfamily 2. The helicase is morepreferably a member of one of the following subfamilies: RecD, Upf1(RNA), PcrA, Rep, UvrD, Hel308, Mtr4 (RNA), XPD, NS3 (RNA), Mss116(RNA), Prp43 (RNA), RecG, RecQ, TIR, RapA and Hef (RNA). The first fiveof those subfamilies are in superfamily 1 and the second elevensubfamilies are in superfamily 2. Members of the Upf1, Mtr4, NS3,Mss116, Prp43 and Hef subfamilies are RNA helicases. Members of theremaining subfamilies are DNA helicases.

The helicase may be a multimeric or oligomeric helicase. In other words,the helicase may need to form a multimer or an oligomer, such as adimer, to function. In such embodiments, the two or more parts cannot beon different monomers. The helicase is preferably monomeric. In otherwords, the helicase preferably does not need to form a multimer or anoligomer, such as a dimer, to function. Hel308, RecD, TraI and XPDhelicases are all monomeric helicases. These are discussed in moredetail below. Methods for determining whether or not a helicase isoligomeric/multimeric or monomeric are known in the art. For instance,the kinetics of radiolabelled or fluorescently-labelled polynucleotideunwinding using the helicase can be examined. Alternatively, thehelicase can be analysed using size exclusion chromatography.

Monomeric helicases may comprise several domains attached together. Forinstance, TraI helicases and TraI subgroup helicases may contain twoRecD helicase domains, a relaxase domain and a C-terminal domain. Thedomains typically form a monomeric helicase that is capable offunctioning without forming oligomers. The two or more parts may bepresent on the same or different domains of a monomeric helicase. Theunmodified helicase suitable for modification in accordance with theinvention is preferably capable of binding to the target polynucleotideat an internal nucleotide. Internal nucleotides are defined above.

Generally, a helicase which is capable of binding at an internalnucleotide is also capable of binding at a terminal nucleotide, but thetendency for some helicases to bind at an internal nucleotide will begreater than others. For an unmodified helicase suitable formodification in accordance with the invention, typically at least 10% ofits binding to a polynucleotide will be at an internal nucleotide.Typically, at least 20%, at least 30%, at least 40% or at least 50% ofits binding will be at an internal nucleotide. Binding at a terminalnucleotide may involve binding to both a terminal nucleotide andadjacent nucleotides at the same time. For the purposes of theinvention, this is not binding to the target polynucleotide at aninternal nucleotide. In other words, the helicase for modification usingthe invention is not only capable of binding to a terminal nucleotide incombination with one or more adjacent internal nucleotides. The helicasemay be capable of binding to an internal nucleotide without concurrentbinding to a terminal nucleotide.

A helicase which is capable of binding at an internal nucleotide maybind to more than one internal nucleotide. Typically, the helicase bindsto at least 2 internal nucleotides, for example at least 3, at least 4,at least 5, at least 10 or at least 15 internal nucleotides. Typicallythe helicase binds to at least 2 adjacent internal nucleotides, forexample at least 3, at least 4, at least 5, at least 10 or at least 15adjacent internal nucleotides. The at least 2 internal nucleotides maybe adjacent or non-adjacent.

If modification in accordance with the invention closes the opening suchthat unbinding from internal nucleotides is prevented, it is preferredthat the unmodified helicase is capable of at least some binding to aterminal nucleotide. This will allow the modified helicase to bind to apolynucleotide at one terminus and control the movement of thepolynucleotide along its entire length without unbinding. The helicasewill eventually unbind from the polynucleotide at the opposite terminusfrom which it became bound.

The ability of a helicase to bind to a polynucleotide at an internalnucleotide may be determined by carrying out a comparative assay. Theability of a helicase to bind to a control polynucleotide A is comparedto the ability to bind to the same polynucleotide but with a blockinggroup attached at the terminal nucleotide (polynucleotide B). Theblocking group prevents any binding at the terminal nucleotide of strandB, and thus allows only internal binding of a helicase. Alternatively,the ability of a helicase to bind to an internal nucleotide may also beassayed using circular polynucleotides.

Examples of helicases which are capable of binding at an internalnucleotide include, but are not limited to, Hel308 Tga, Hel308 Mhu andHel308 Csy. Hence, the helicase preferably comprises (a) the sequence ofHel308 Tga (i.e. SEQ ID NO: 33) or a variant thereof or (b) the sequenceof Hel308 Csy (i.e. SEQ ID NO: 22) or a variant thereof or (c) thesequence of Hel308 Mhu (i.e. SEQ ID NO: 52) or a variant thereof.Variants of these sequences are discussed in more detail below. Variantspreferably comprise one or more substituted cysteine residues and/or oneor more substituted Faz residues to facilitate attachment as discussedabove.

The helicase is preferably a Hel308 helicase. Any Hel308 helicase may beused in accordance with the invention. Hel308 helicases are also knownas ski2-like helicases and the two terms can be used interchangeably.Suitable Hel308 helicases are disclosed in Table 4 of US PatentApplication Nos. 61,549,998 and 61/599,244 and International ApplicationNo. PCT/GB2012/052579 (published as WO 2013/057495).

The Hel308 helicase typically comprises the amino acid motifQ-X1-X2-G-R-A-G-R (hereinafter called the Hel308 motif, SEQ ID NO: 8).The Hel308 motif is typically part of the helicase motif VI (Tuteja andTuteja, Eur. J. Biochem. 271, 1849-1863 (2004)). X1 may be C, M or L. X1is preferably C. X2 may be any amino acid residue. X2 is typically ahydrophobic or neutral residue. X2 may be A, F, M, C, V, L, I, S, T, Por R. X2 is preferably A, F, M, C, V, L, I, S, T or P. X2 is morepreferably A, M or L. X2 is most preferably A or M.

The Hel308 helicase preferably comprises the motif Q-X1-X2-G-R-A-G-R-P(hereinafter called the extended Hel308 motif, SEQ ID NO: 9) wherein X1and X2 are as described above.

The most preferred Hel308 helicases, Hel308 motifs and extended Hel308motifs are shown in the Table 1 below.

TABLE 1 Preferred Hel308 helicases and their motifs SEQ % % ExtendedID NO: Helicase Names Identity Identity Hel308 motif Hel308 motif Hel308Hel308 Pfu Mbu 10 Hel308 Mbu Methanococcoides 37% — QMAGRAGR QMAGRAGRPburtonii (SEQ ID NO: 11) (SEQ ID NO: 12) 13 Hel308 Pfu Pyrococcus — 37%QMLGRAGR QMLGRAGRP furiosus DSM 3638 (SEQ ID NO: 14) (SEQ ID NO: 15) 16Hel308 Hvo Haloferax volcanii 34% 41% QMMGRAGR QMMGRAGRP (SEQ ID NO: 17)(SEQ ID NO: 18) 19 Hel308 Hla Halorubrum 35% 42% QMCGRAGR QMCGRAGRPlacusprofundi (SEQ ID NO: 20) (SEQ ID NO: 21) 22 Hel308 Csy Cenarchaeum34% 34% QLCGRAGR QLCGRAGRP symbiosum (SEQ ID NO: 23) (SEQ ID NO: 24) 25Hel308 Sso Sulfolobus 35% 33% QMSGRAGR QMSGRAGRP solfataricus(SEQ ID NO: 26) (SEQ ID NO: 27) 28 Hel308 Mfr Methanogenium 37% 44%QMAGRAGR QMAGRAGRP frigidum (SEQ ID NO: 11) (SEQ ID NO: 12) 29Hel308 Mok Methanothermococcus 37% 34% QCIGRAGR QCIGRAGRP okinawensis(SEQ ID NO: 30) (SEQ ID NO: 31) 32 Hel308 Mig Methanotorris 40% 35%QCIGRAGR QCIGRAGRP igneus Kol 5 (SEQ ID NO: 30) (SEQ ID NO: 31) 33Hel308 Tga Thermococcus 60% 38% QMMGRAGR QMMGRAGRP gammatolerans EJ3(SEQ ID NO: 17) (SEQ ID NO: 18) 34 Hel308 Tba Thermococcus 57% 35%QMIGRAGR QMIGRAGRP barophilus MP (SEQ ID NO: 35) (SEQ ID NO: 36) 37Hel308 Tsi Thermococcus 56% 35% QMMGRAGR QMMGRAGRP sibiricus MM 739(SEQ ID NO: 17) (SEQ ID NO: 18) 38 Hel308 Mba Methanosarcina 39% 60%QMAGRAGR QMAGRAGRP barkeri str. Fusaro (SEQ ID NO: 11) (SEQ ID NO: 12)39 Hel308 Mac Methanosarcina 38% 60% QMAGRAGR QMAGRAGRP acetivorans(SEQ ID NO: 11) (SEQ ID NO: 12) 40 Hel308 Mmah Methanohalophilus 38% 60%QMAGRAGR QMAGRAGRP mahii DSM 5219 (SEQ ID NO: 11) (SEQ ID NO: 12) 41Hel308 Mmaz Methanosarcina 38% 60% QMAGRAGR QMAGRAGRP mazei(SEQ ID NO: 11) (SEQ ID NO: 12) 42 Hel308 Mth Methanosaeta 39% 46%QMAGRAGR QMAGRAGRP thermophila PT (SEQ ID NO: 11) (SEQ ID NO: 12) 43Hel308 Mzh Methanosalsum 39% 57% QMAGRAGR QMAGRAGRP zhilinae DSM 4017(SEQ ID NO: 11) (SEQ ID NO: 12) 44 Hel308 Mev Methanohalobium 38% 61%QMAGRAGR QMAGRAGRP evestigatum Z-7303 (SEQ ID NO: 11) (SEQ ID NO: 12) 45Hel308 Mma Methanococcus 36% 32% QCIGRAGR QCIGRAGRP maripaludis(SEQ ID NO: 30) (SEQ ID NO: 31) 46 Hel308 Nma Natriaalba magadii 37% 43%QMMGRAGR QMMGRAGRP (SEQ ID NO: 17) (SEQ ID NO: 18) 47 Hel308 MboMethanoregula 38% 45% QMAGRAGR QMAGRAGRP boonei 6A8 (SEQ ID NO: 11)(SEQ ID NO: 12) 48 Hel308 Fac Ferroplasma 34% 32% QMIGRAGR QMIGRAGRPacidarmanus (SEQ ID NO: 35) (SEQ ID NO: 36) 49 Hel308 MfeMethanocaldococcus 40% 35% QCIGRAGR QCIGRAGRP fervens AG86(SEQ ID NO: 30) (SEQ ID NO: 31) 50 Hel308 Mja Methanocaldococcus 24% 22%QCIGRAGR QCIGRAGRP jannaschii (SEQ ID NO: 30) (SEQ ID NO: 31) 51Hel308 Min Methanocaldococcus 41% 33% QCIGRAGR QCIGRAGRP infernus(SEQ ID NO: 30) (SEQ ID NO: 31) 52 Hel308 Mhu Methanospirillum 36% 40%QMAGRAGR QMAGRAGRP hungatei JF-1 (SEQ ID NO: 11) (SEQ ID NO: 12) 53Hel308 Afu Archaeoglobus 40% 40% QMAGRAGR QMAGRAGRP fulgidus DSM 4304(SEQ ID NO: 11) (SEQ ID NO: 12) 54 Hel308 Htu Haloterrigcna 35% 43%QMAGRAGR QMAGRAGRP turkmenica (SEQ ID NO: 11) (SEQ ID NO: 12) 55Hel308 Hpa Haladaptatus 38% 45% QMFGRAGR QMFGRAGRP paucihalophilus(SEQ ID NO: 56) (SEQ ID NO: 57) DX253 58 Hel308 Hsp Halobacterium sp.  36.8%   42.0% QMFGRAGR QMFGRAGRP ski2-like NRC-1 (SEQ ID NO: 56)(SEQ ID NO: 57) helicase

The most preferred Hel308 motif is shown in SEQ ID NO: 17. The mostpreferred extended Hel308 motif is shown in SEQ ID NO: 18.

The Hel308 helicase preferably comprises the sequence of SEQ ID NO: 10,13, 16, 19, 22, 25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 44,45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 or 58 or a variant thereof.

In Hel308 helicases, the polynucleotide domain and opening can be foundbetween domain (one of the ATPase domains) and domain 4 (the ratchetdomain) and domain 2 and domain (the molecular brake). The two or moreparts connected in accordance with the invention are preferably (a) anyamino acid in domain 2 and any amino acid in domain 4 or (b) any aminoacid in domain 2 and any amino acid in domain 5. The amino acid residueswhich define domains 2, 4 and 5 in various Hel308 helicases are listedin Table 2 below.

TABLE 2 Amino acid residues which correspond to domains 2, 4 and 5 invarious Hel 308 helicases SEQ ID Hel308 Domain 2 Domain 4 Domain 5 NO:Homologue Start End Start End Start End 10 Mbu W200 E409 Y506 G669 S670Q760 13 Pfu W198 F398 Y490 G640 I641 S720 16 Hvo W201 W418 Y509 G725V726 E827 19 Hla W201 W418 Y513 G725 V726 R824 22 Csy W205 G414 Y504G644 I645 K705 25 Sso W204 L420 Y506 G651 I652 S717 28 Mfr W193 E397Y488 G630 I631 I684 29 Mok W198 G415 Y551 G706 A707 I775 32 Mig W200E408 Y495 G632 A633 I699 33 Tga W198 R399 Y491 G639 V640 R720 34 TbaW219 F420 Y512 G660 V661 K755 37 Tsi W221 L422 Y514 G662 V663 K744 38Mba W200 E409 Y498 G643 A644 Y729 39 Mac W200 E409 Y499 G644 A645 F73040 Mmah W196 G405 Y531 G678 A679 N747 41 Mmaz W200 E409 Y499 G644 A645Y730 42 Mth W203 M404 Y491 G629 A630 A693 43 Mzh W200 N409 Y505 G651I652 T739 44 Mev W200 D409 Y499 G643 V644 F733 45 Mma W196 G405 Y531G678 A679 N747 46 Nma W201 W413 Y541 G688 V689 F799 47 Mbo W197 E402Y493 G637 I638 G723 48 Fac F197 T390 Y480 G613 V614 R681 49 Mfe W199Q408 Y494 G629 A630 F696 50 Mja W197 Q406 Y492 G627 A628 F694 51 MinW189 Q390 Y476 G604 A605 I670 52 Mhu W198 D402 Y493 G637 V638 C799 53Afu W201 F399 Y487 G626 V627 E696 54 Htu W201 W413 Y533 G680 V681 F79155 Hpa W201 W412 Y502 G657 V658 E752 58 Hsp (ski2- W210 Y421 Y512 G687V688 S783 like helicase)

The Hel308 helicase preferably comprises the sequence of Hel308 Mbu(i.e. SEQ ID NO: 10) or a variant thereof. In Hel308 Mbu, thepolynucleotide domain and opening can be found between domain 2 (one ofthe ATPase domains) and domain 4 (the ratchet domain) and domain 2 anddomain 5 (the molecular brake). The two or more parts of Hel308 Mbuconnected are preferably (a) any amino acid in domain 2 and any aminoacid in domain 4 or (b) any amino acid in domain 2 and any amino acid indomain 5. The amino acid residues which define domains 2, 4 and 5 forHel308 Mbu are listed in Table 2 above. The two or more parts of Hel308Mbu connected are preferably amino acids 284 and 615 in SEQ ID NO: 10.These amino acids are preferably substituted with cysteine (i.e. E284Cand S615C) such that they can be connected by cysteine linkage.

The invention also provides a mutant Hel308 Mbu protein which comprisesa variant of SEQ ID NO: 10 in which E284 and S615 are modified. E284 andS615 are preferably substituted. E284 and S615 are more preferablysubstituted with cysteine (i.e. E284C and S615C). The variant may differfrom SEQ ID NO: 10 at positions other than E284 and S615 as long as E284and S615 are modified. The variant will preferably be at least 30%homologous to SEQ ID NO: 10 based on amino acid identity as discussed inmore detail below. E284 and S615 are not connected. The mutant Hel308Mbu protein of the invention may be used to form a modified helicase ofthe invention in which E284 and S615 are connected.

The Hel308 helicase more preferably comprises (a) the sequence of Hel308Tga (i.e. SEQ ID NO: 33) or a variant thereof, (b) the sequence ofHel308 Csy (i.e. SEQ ID NO: 22) or a variant thereof or (c) the sequenceof Hel308 Mhu (i.e. SEQ ID NO: 52) or a variant thereof.

A variant of a Hel308 helicase is an enzyme that has an amino acidsequence which varies from that of the wild-type helicase and whichretains polynucleotide binding activity. In particular, a variant of SEQID NO: 10, 13, 16, 19, 22, 25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41,42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 or 58 is anenzyme that has an amino acid sequence which varies from that of SEQ IDNO: 10, 13, 16, 19, 22, 25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42,43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 or 58 and whichretains polynucleotide binding activity. Polynucleotide binding activitycan be determined using methods known in the art. Suitable methodsinclude, but are not limited to, fluorescence anisotropy, tryptophanfluorescence and electrophoretic mobility shift assay (EMSA). Forinstance, the ability of a variant to bind a single strandedpolynucleotide can be determined as described in the Examples.

The variant retains helicase activity. This can be measured in variousways. For instance, the ability of the variant to translocate along apolynucleotide can be measured using electrophysiology, a fluorescenceassay or ATP hydrolysis.

The variant may include modifications that facilitate handling of thepolynucleotide encoding the helicase and/or facilitate its activity athigh salt concentrations and/or room temperature. Variants typicallydiffer from the wild-type helicase in regions outside of the Hel308motif or extended Hel308 motif discussed above. However, variants mayinclude modifications within these motif(s).

Over the entire length of the amino acid sequence of SEQ ID NO: 10, 13,16, 19, 22, 25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 44, 45,46, 47, 48, 49, 50, 51, 52, 53, 54, 55 or 58, a variant will preferablybe at least 30% homologous to that sequence based on amino acididentity. More preferably, the variant polypeptide may be at least 40%,at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, atleast 70%, at least 75%, at least 80%, at least 85%, at least 90% andmore preferably at least 95%, 97% or 99% homologous based on amino acididentity to the amino acid sequence of SEQ ID NO: 10, 13, 16, 19, 22,25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48,49, 50, 51, 52, 53, 54, 55 or 58 over the entire sequence. There may beat least 70%, for example at least 80%, at least 85%, at least 90% or atleast 95%, amino acid identity over a stretch of 150 or more, forexample 200, 300, 400, 500, 600, 700, 800, 900 or 1000 or more,contiguous amino acids (“hard homology”). Homology is determined asdescribed below. The variant may differ from the wild-type sequence inany of the ways discussed below with reference to SEQ ID NOs: 2 and 4.

A variant of SEQ ID NO: 10, 13, 16, 19, 22, 25, 28, 29, 32, 33, 34, 37,38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55or 58 preferably comprises the Hel308 motif or extended Hel308 motif ofthe wild-type sequence as shown in Table 1 above. However, a variant maycomprise the Hel308 motif or extended Hel308 motif from a differentwild-type sequence. For instance, a variant of SEQ ID NO: 10 maycomprise the Hel308 motif or extended Hel308 motif from SEQ ID NO: 13(i.e. SEQ ID NO: 14 or 15). Variants of SEQ ID NO: 10, 13, 16, 19, 22,25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48,49, 50, 51, 52, 53, 54, 55 or 58 may also include modifications withinthe Hel308 motif or extended Hel308 motif of the relevant wild-typesequence. Suitable modifications at X1 and X2 are discussed above whendefining the two motifs. A variant of SEQ ID NO: 10, 13, 16, 19, 22, 25,28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49,50, 51, 52, 53, 54, 55 or 58 preferably comprises one or moresubstituted cysteine residues and/or one or more substituted Fazresidues to facilitate attachment as discussed above.

A variant of SEQ ID NO: 10 may lack the first 19 amino acids of SEQ IDNO: 10 and/or lack the last 33 amino acids of SEQ ID NO: 10. A variantof SEQ ID NO: 10 preferably comprises a sequence which is at least 70%,at least 75%, at least 80%, at least 85%, at least 90% or morepreferably at least 95%, at least 97% or at least 99% homologous basedon amino acid identity with amino acids 20 to 211 or 20 to 727 of SEQ IDNO: 10.

SEQ ID NO: 10 (Hel308 Mbu) contains five natural cysteine residues.However, all of these residues are located within or around the DNAbinding grove of the enzyme. Once a DNA strand is bound within theenzyme, these natural cysteine residues become less accessible forexternal modifications. This allows specific cysteine mutants of SEQ IDNO: 10 to be designed and attached to the moiety using cysteine linkageas discussed above. Preferred variants of SEQ ID NO: 10 have one or moreof the following substitutions: A29C, Q221C, Q442C, T569C, A577C, A700Cand S708C. The introduction of a cysteine residue at one or more ofthese positions facilitates cysteine linkage as discussed above. Otherpreferred variants of SEQ ID NO: 10 have one or more of the followingsubstitutions: M2Faz, R10Faz, F15Faz, A29Faz, R185Faz, A268Faz, E284Faz,Y387Faz, F400Faz, Y455Faz, E464Faz, E573Faz, A577Faz, E649Faz, A700Faz,Y720Faz, Q442Faz and S708Faz. The introduction of a Faz residue at oneor more of these positions facilitates Faz linkage as discussed above.

The helicase is preferably a RecD helicase. Any RecD helicase may beused in accordance with the invention. The structures of RecD helicasesare known in the art (FEBS J. 2008 April; 275(8):1835-51. Epub 2008 Mar.9. ATPase activity of RecD is essential for growth of the AntarcticPseudomonas syringae Lz4W at low temperature. Satapathy A K, PavankuniarT L, Bhattacharya, Sankaranarayanan R, Ray MK; EMS Microbiol Rev. 2009May; 33(3):657-87. The diversity of conjugative relaxases and itsapplication in plasmid classification. Garcillan-Barcia M P, Francia MV, de la Cruz F, J Biol Chem. 2011 Apr. 8; 286(14):12670-82. Epub 2011Feb. 2. Functional characterization of the multidomain F plasmid TraIrelaxase-helicase. Cheng Y, McNamara D E, Miley M J, Nash R P, Redinbo MR).

The RecD helicase typically comprises the amino acid motifX1-X2-X3-G-X4-X5-X6-X7 (hereinafter called the RecD-like motif I; SEQ IDNO: 59), wherein X1 is G, S or A, X2 is any amino acid, X3 is P, A, S orG, X4 is T, A, V, S or C, X5 is G or A, X6 is K or R and X7 is T or S.X1 is preferably G. X2 is preferably G, I, Y or A. X2 is more preferablyG. X3 is preferably P or A. X4 is preferably T, A, V or C. X4 ispreferably T, V or C X5 is preferably G. X6 is preferably K. X7 ispreferably T or S. The RecD helicase preferably comprisesQ-(X8)₁₆₋₁₈-X1-X2-X3-G-X4-X5-X6-X7 (hereinafter called the extendedRecD-like motif I, SEQ ID NOs: 60, 61 and 62), wherein X1 to X7 are asdefined above and X8 is any amino acid. There are preferably 16 X8residues (i.e. (X8)₁₆) in the extended RecD-like motif I (SEQ ID NO:60). Suitable sequences for (X8)₁₆ can be identified in SEQ ID NOs: 14,17, 20, 23, 26, 29, 32, 35, 38, 41, 44, 47 and 50 of U.S. PatentApplication No. 61/581,332 and SEQ ID NOs: 18, 21, 24, 25, 28, 30, 32,35, 37, 39, 41, 42 and 44 of International Application No.PCT/GB2012/053274 (published as WO 2012/098562).

The RecD helicase preferably comprises the amino acid motifG-G-P-G-Xa-G-K-Xb (hereinafter called the RecD motif I; SEQ ID NO: 63)wherein Xa is T, V or C and Xb is T or S. Xa is preferably T. Xb ispreferably T, The Rec-D helicase preferably comprises the sequenceG-G-P-G-T-G-K-T (SEQ ID NO: 64). The RecD helicase more preferablycomprises the amino acid motif Q-(X8)₁₆₋₁₈-G-G-P-G-Xa-G-K-Xb(hereinafter called the extended RecD motif I: SEQ ID NO: 65, 66 and67), wherein Xa and Xb are as defined above and X8 is any amino acid.There are preferably 16 X8 residues (i.e. (X8)₁₆) in the extended RecDmotif I (SEQ ID NO: 65) Suitable sequences for (X8)₁₆ can be identifiedin SEQ ID NOs: 14, 17, 20, 23, 26, 29, 32, 35, 38, 41, 44, 47 and 50 ofU.S. Patent Application No. 61/581,332 and SEQ ID NOs: 18, 21, 24, 25,28, 30, 32, 35, 37, 39, 41, 42 and 44 of International Application No.PCT/GB2012/053274 (published as WO 2012/098562).

The RecD helicase typically comprises the amino acid motifX1-X2-X3-X4-X5-(X6)₃-Q-X7 (hereinafter called the RecD-like motif V: SEQID NO: 68), wherein X is Y, W or F, X2 is A., T, S. M, C or V, X3 is anyamino acid, X4 is T, N or S, X5 is A, T, G, S, V or I, X6 is any aminoacid and X7 is G or S. X1 is preferably Y. X2 is preferably A, M, C orV. X2 is more preferably A X3 is preferably, I, M or L. X3 is morepreferably I or L. X4 is preferably T or S. X4 is more preferably T. 5is preferably A, V or I. X is more preferably V or I. X5 is mostpreferably V. (X6)₃ is preferably H-K-S, H-M-A, H-G-A or H-R-S. (X6)₃ ismore preferably H-K-S. X7 is preferably G. The RecD helicase preferablycomprises the amino acid motif Xa-Xb-Xc-Xd-Xe-H-K-S-Q-G (hereinaftercalled the RecD motif V; SEQ ID NO: 69), wherein Xa is Y, W or F, Xb isA, M, C or V, Xc is I, M or L, Xd is T or S and Xe is V or I. Xa ispreferably Y. Xb is preferably A. Xd is preferably T. Xd is preferablyV. Preferred RecD motifs I are shown in Table 5 of U.S. PatentApplication No. 61/581,332. Preferred RecD-like motifs I are shown inTable 7 of U.S. Patent Application No. 61/581,332 and InternationalApplication No. PCT/GB2012/053274 (published as WO 2012/098562).Preferred RecD-like motifs V are shown in Tables 5 and 7 of U.S. PatentApplication No. 61/581,332 and International Application No.PCT/GB2012/053274 (published as WO 2012/098562).

The RecD helicase is preferably one of the helicases shown in Table 4 or5 of U.S. Patent Application No. 61/581,332 and InternationalApplication No. PCT/GB2012/053274 (published as WO 2012/098562) or avariant thereof. Variants are described in U.S. Patent Application No.61/581,332 and International Application No. PCT/GB2012/053274(published as WO 2012/098562).

The RecD helicase is preferably a TraI helicase or a TraI subgrouphelicase. TraI helicases and TraI subgroup helicases may contain twoRecD helicase domains, a relaxase domain and a C-terminal domain. TheTraI subgroup helicase is preferably a TrwC helicase. The TraI helicaseor TraI subgroup helicase is preferably one of the helicases shown inTable 6 of U.S. Patent Application No. 61/581,332 and InternationalApplication No. PCT/GB2012/053274 (published as WO 2012/098562) or avariant thereof. Variants are described in U.S. Patent Application No.61/581,332 and International Application No. PCT/GB2012/053274(published as WO 2012/098562).

The TraI helicase or a TraI subgroup helicase typically comprises aRecD-like motif I as defined above (SEQ ID NO 59) and/or a RecD-likemotif V as defined above (SEQ ID NO: 68) The TraI helicase or a TraIsubgroup helicase preferably comprises both a RecD-like motif I (SEQ IDNO: 59) and a RecD-like motif V (SEQ ID NO: 68). The TraI helicase or aTraI subgroup helicase typically further comprises one of the followingtwo motifs:

-   -   The amino acid motif H-(X1)₂-X2-R-(X3)₃₋₁₂-H-X4-H (hereinafter        called the MobF motif III; SEQ ID NOs: 70 to 77) wherein X1 and        X2 are any amino acid and X2 and X4 are independently selected        from any amino acid except D, E, K and R. (X1)₂ is of course        X1a-X1b. X1a and Xb can be the same of different amino acid. X1a        is preferably D or E. Xb is preferably T or D. (X1)₂ is        preferably DT or ED. (X1)₂ is most preferably DT. The 5 to 12        amino acids in (X3)₅₋₁₂ can be the same or different. X2 and X4        are independently selected from G, P, A, V, L, I, M, C, F, Y, W,        H, Q, N, S and T. X2 and X4 are preferably not charged. X2 and        X4 are preferably not H. X2 is more preferably N, S or A. X2 is        most preferably N. X4 is most preferably F or T. (X3)₅₋₁₂ is        preferably 6 or 10 residues in length. Suitable embodiments of        (X3)₅₋₁₂ can be derived from SEQ ID NOs: 58, 62, 66 and 70 shown        in Table 7 of U.S. Patent Application No. 61/581,332 and SEQ ID        NOs: 61, 65, 69, 73, 74, 82, 86, 90, 94, 98, 102, 110, 112, 113,        114, 117, 121, 124, 125, 129, 133, 136, 140, 144, 147, 151, 152,        156, 160, 164 and 168 of International Application No.        PCT/GB2012/053274 (published as WO 2012/098562).    -   The amino acid motif G-X1-X2-X3-X4-X5-X6-X7-H-(X8)₆₋₁₂-H-X9        (hereinafter called the MobQ motif III; SEQ ID NOs: 78 to 84),        wherein X1, X3, X5, X6, X7 and X9 are independently selected        from any amino acid except D, E, K and R, X4 is D or E and X8 is        any amino acid. X1, X2, X3, X5, X6, X7 and X9 are independently        selected from G, P, A, V, L, I, M, C, F, Y, W, H, Q, N, S and T.        X1, X2, X3, X5, X6, X7 and X9 are preferably not charged. X1,        X2, X3, X5, X6, X7 and X9 are preferably not H. The 6 to 12        amino acids in (X8)₆₋₁₂ can be the same or different. Preferred        MobF motifs III are shown in Table 7 of U.S. Patent Application        No. 61/581,332 and International Application No.        PCT/GB2012/053274 (published as WO 2012/098562).

The TraI helicase or TraI subgroup helicase is more preferably one ofthe helicases shown in Table 6 or 7 of U.S. Patent Application No.61/581,332 and International Application No. PCT/GB2012/053274(published as WO 2012/098562) or a variant thereof. The TraI helicasemost preferably comprises the sequence shown in SEQ ID NO: 85 or avariant thereof. SEQ ID NO: 85 is TraI Eco (NCBI Reference Sequence:NP_061483.1; Genbank AAQ98619.1; SEQ ID NO: 85). TraI Eco comprises thefollowing motifs: RecD-like motif I (GYAGVGKT; SEQ ID NO: 86), RecD-likemotif V (YAITAHGAQG; SEQ ID NO: 87) and Mob F motif III (HDTSRDQEPQLHTH;SEQ ID NO: 88).

The TraI helicase or TraI subgroup helicase more preferably comprisesthe sequence of one of the helicases shown in Table 3 below, i.e. one ofSEQ ID NOs: 85, 126, 134 and 138, or a variant thereof.

TABLE 3 More preferred TraI helicase and TraI subgroup helicases %Identity RecD-like RecD-like Mob F SEQ to TraI motif I motif V motif IIIID NO Name Strain NCBI ref Eco (SEQ ID NO: ) (SEQ ID NO: ) (SEQ ID NO: ) 85 TraI Escherichia coli NCBI — GYAGVGKT YAITAHGAQG HDTSRDQEPQLHTH EcoReference (86) (87) 88) Sequence: NP_061483.1 GenBank AAQ98619.1 126TrwC Citromicrobium NCBI 15% GIAGAGKS YALNVHMAQG HDTNRNQEPNLHFH Cbabathyomarinum Reference (131) (132) (133) JL354 Sequence: ZP_06861556.1134 TrwC Halothiooacillus NCBI   11.5% GAAGAGKT YCITIHRSQGHEDARTVDDIADPQ Hne neapolitanus Reference (135) (136) LHTH C2 Sequence:(137) YP_003262832.1 138 TrwC Erythrobacter NCBI 16% GIAGAGKS YALNAHMAQGNDTNRNQEPNLHFH Eli litoralis Reference (131) (139) (133) HTCC2594Sequence: YP_457045.1

The two or more parts of TrwC Cba connected are preferably (a) aminoacids 691 and 346 in SEQ ID NO: 126; (b) amino acids 657 and 339 in SEQID NO: 126; (c) amino acids 691 and 350 in SEQ ID NO: 126; or (d) aminoacids 690 and 350 in SEQ ID NO: 126. These amino acids are preferablysubstituted with cysteine such that they can be connected by cysteinelinkage.

The invention also provides a mutant TrwC Cba protein which comprises avariant of SEQ ID NO: 126 in which amino acids 691 and 346; 657 and 339;691 and 350; or 690 and 350 are modified. The amino acids are preferablysubstituted. The amino acids are more preferably substituted withcysteine. The variant may differ from SEQ ID NO: 126 at positions otherthan 691 and 346; 657 and 339; 691 and 350; or 690 and 350 as long asthe relevant amino acids are modified. The variant will preferably be atleast 10% homologous to SEQ ID NO: 126 based on amino acid identity asdiscussed in more detail below. Amino acid 691 and 346; 657 and 339; 691and 350; or 690 and 350 are not connected. The mutant TrwC Cba proteinof the invention may be used to form a modified helicase of theinvention in which the modified amino acids are connected.

A variant of a RecD helicase, TraI helicase or TraI subgroup helicase isan enzyme that has an amino acid sequence which varies from that of thewild-type helicase and which retains polynucleotide binding activity.This can be measured as described above. In particular, a variant of SEQID NO: 85, 126, 134 or 138 is an enzyme that has an amino acid sequencewhich varies from that of SEQ ID NO: 85, 126, 134 or 138 and whichretains polynucleotide binding activity. The variant retains helicaseactivity. The variant must work in at least one of the two modesdiscussed below. Preferably, the variant works in both modes. Thevariant may include modifications that facilitate handling of thepolynucleotide encoding the helicase and/or facilitate its activity athigh salt concentrations and/or room temperature. Variants typicallydiffer from the wild-type helicase in regions outside of the motifsdiscussed above. However, variants may include modifications withinthese motif(s).

Over the entire length of the amino acid sequence of any one of SEQ IDNO: 85, 126, 134 and 138, a variant will preferably be at least 10%homologous to that sequence based on amino acid identity. Morepreferably, the variant polypeptide may be at least 20%, at least 25%,at least 30%, at least 40%, at least 45%, at least 50%, at least 55%, atleast 60%, at least 65%, at least 70%, at least 75%, at least 80%, atleast 85%, at least 90% and more preferably at least 95%, 97% or 99%homologous based on amino acid identity to the amino acid sequence ofany one of SEQ ID NOs: 85, 126, 134 and 138 over the entire sequence.There may be at least 70%, for example at least 80%, at least 85%, atleast 90% or at least 95%, amino acid identity over a stretch of 150 ormore, for example 200, 300, 400, 500, 600, 700, 800, 900 or 1000 ormore, contiguous amino acids (“hard homology”). Homology is determinedas described below. The variant may differ from the wild-type sequencein any of the ways discussed above with reference to SEQ ID NOs: 2 and4.

A variant of any one of SEQ ID NOs: 85, 126, 134 and 138 preferablycomprises the RecD-like motif I and/or RecD-like motif V of thewild-type sequence. However, a variant of SEQ ID NO: 85, 126, 134 or 138may comprise the RecD-like motif I and/or extended RecD-like motif Vfrom a different wild-type sequence. For instance, a variant maycomprise any one of the preferred motifs shown in Tables 5 and 7 of U.S.Patent Application No. 61/581,332 and International Application No.PCT/GB2012/053274 (published as WO 2012/098562). Variants of SEQ ID NOs:85, 126, 134 and 138 may also include modifications within the RecD-likemotifs I and V of the wild-type sequence. A variant of SEQ ID NO: 85.126, 134 or 138 preferably comprises one or more substituted cysteineresidues and/or one or more substituted Faz residues to facilitateattachment as discussed above.

The helicase is preferably an XPD helicase. Any XPD helicase may be usedin accordance with the invention. XPD helicases are also known as Rad3helicases and the two terms can be used interchangeably.

The structures of XPD helicases are known in the art (Cell. 2008 May 30;133(5):801-12. Structure of the DNA repair helicase XPD. Liu H, RudolfJ, Johnson K A, McMahon S A, Oke M, Carter L, McRobbie A M, Brown S E,Naismith J H, White M F). The XPD helicase typically comprises the aminoacid motif X1-X2-X3-G-X4-X5-X6-E-G (hereinafter called XPD motif V; SEQID NO: 89). X1, X2, X5 and X6 are independently selected from any aminoacid except D, E, K and R, X1, X2, X5 and X6 are independently selectedfrom G, P, A, V, L, I. M, C, F, Y, W, H, Q, N, S and T. X1, X2, X5 andX6 are preferably not charged. X1, X2, X5 and X6 are preferably not H.X1 is more preferably V, L, I, S or Y. X5 is more preferably V, L, I, Nor F X6 is more preferably S or A. X3 and X4 may be any amino acidresidue. X4 is preferably K, R or T.

The XPD helicase typically comprises the amino acid motifQ-Xa-Xb-G-R-Xc-Xd-R (Xe)₃-Xf-(Xg)-D-Xh-R (hereinafter called D motif VI;SEQ ID NO: 90). Xa, Xe and Xg may be any amino acid residue. Xb, Xc andXd are independently selected from any amino acid except D, E, K and R.Xb, Xc and Xd are typically independently selected from G, P, A, V, L,I, M, C, F, Y, W, H, Q, N, S and T Xb, Xc and Xd are preferably notcharged. Xb, Xc and Xd are preferably not H. Xb is more preferably V, A,L, I or M. Xc is more preferably V, A, L, I, M or C. Xd is morepreferably I, H, L, F, M or V. Xf may be D or E. (Xg)₇ is X_(g1),X_(g2), X_(g3), X_(g4), X_(g5), X_(g6) and X_(g7). X_(g2) is preferablyG, A, S or C. X_(g5) is preferably F, V L, I, M, A, W or Y. X_(g6) ispreferably L, F, Y, M, I or V. X_(g7) is preferably A, C, V, L, I, M orS.

The XPD helicase preferably comprises XPD motifs V and VI. The mostpreferred XPD motifs V and VI are shown in Table 5 of U.S. PatentApplication No. 61/581,340 and International Application No.PCT/GB2012/053273 (published as WO 2012/098561).

The XPD helicase preferably further comprises an iron sulphide (FeS)core between two Walker A and B motifs (motifs I and II). An FeS coretypically comprises an iron atom coordinated between the sulphide groupsof cysteine residues. The FeS core is typically tetrahedral.

The XPD helicase is preferably one of the helicases shown in Table 4 or5 of U.S. Patent Application No. 61/581,340 and InternationalApplication No. PCT/GB2012/053273 (published as WO 2012/098561) or avariant thereof. The XPD helicase most preferably comprises the sequenceshown in SEQ ID NO: 91 or a variant thereof. SEQ ID NO: 91 is XPD Mbu(Methanococcoides burtonii; YP_566221.1; GI:91773529). XPD Mbu comprisesYLWGTLSEG (Motif V; SEQ ID NO: 92) and QAMGRVVRSPTDYGARILLDGR (Motif VI;SEQ ID NO: 93).

A variant of a XPD helicase is an enzyme that has an amino acid sequencewhich varies from that of the wild-type helicase and which retainspolynucleotide binding activity. This can be measured as describedabove. In particular, a variant of SEQ ID NO: 91 is an enzyme that hasan amino acid sequence which varies from that of SEQ ID NO: 91 and whichretains polynucleotide binding activity. The variant retains helicaseactivity. The variant must work in at least one of the two modesdiscussed below. Preferably, the variant works in both modes. Thevariant may include modifications that facilitate handling of thepolynucleotide encoding the helicase and/or facilitate its activity athigh salt concentrations and/or room temperature. Variants typicallydiffer from the wild-type helicase in regions outside of XPD motifs Vand VI discussed above. However, variants may include modificationswithin one or both of these motifs.

Over the entire length of the amino acid sequence of SEQ ID NO: 91, suchas SEQ ID NO: 10, a variant will preferably be at least 10%, preferably30% homologous to that sequence based on amino acid identity. Morepreferably, the variant polypeptide may be at least 40%, at least 45%,at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, atleast 75%, at least 80%, at least 85%, at least 90% and more preferablyat least 95%, 97% or 99% homologous based on amino acid identity to theamino acid sequence of SEQ ID NO: 91 over the entire sequence. There maybe at least 70%, for example at least 80%, at least 85%, at least 90% orat least 95%, amino acid identity over a stretch of 150 or more, forexample 200, 300, 400, 500, 600, 700, 800, 900 or 1000 or more,contiguous amino acids (“hard homology”). Homology is determined asdescribed below. The variant may differ from the wild-type sequence inany of the ways discussed above with reference to SEQ ID NOs: 2 and 4.

A variant of SEQ ID NO: 91 preferably comprises the XPD motif V and/orthe XPD motif VI of the wild-type sequence. A variant of SEQ ID NO: 91more preferably comprises both XPD motifs V and VI of SEQ ID NO: 91.However, a variant of SEQ ID NO: 91 may comprise XPD motifs V and/or VIfrom a different wild-type sequence. For instance, a variant of SEQ IDNO: 91 may comprise any one of the preferred motifs shown in Table 5 ofU.S. Patent Application No. 61/581,340 and International Application No.PCT/GB2012/053273 (published as WO 2012/098561). Variants of SEQ ID NO:91 may also include modifications within XPD motif V and/or XPD motif VIof the wild-type sequence. Suitable modifications to these motifs arediscussed above when defining the two motifs. A variant of SEQ ID NO: 91preferably comprises one or more substituted cysteine residues and/orone or more substituted Faz residues to facilitate attachment asdiscussed above.

Modified Hel308 Helicases

The present invention also provides a modified Hel308 helicase that isuseful for controlling the movement of a polynucleotide. In accordancewith the invention, the helicase is modified by the introduction of oneor more cysteine residues and/or one or more non-natural amino acids atone or more of the positions which correspond to D272, N273, D274, G281,E284, E285, E287, S288, T289, G290, E291, D293, T294, N300, R303, K304,N314, S315, N316, H317, R318, K319, L320, E322, R326, N328, S615, K717,Y720, N721 and S724 in Hel308 Mbu (SEQ ID NO: 10), wherein the helicaseretains its ability to control the movement of a polynucleotide. The oneor more cysteine residues and/or one or more non-natural amino acids arepreferably introduced by substitution.

These modifications do not prevent the helicase from binding to apolynucleotide. For instance, the helicase may bind to a polynucleotidevia internal nucleotides or at one of its termini. These modificationsdecrease the ability of the polynucleotide to unbind or disengage fromthe helicase, particularly from internal nucleotides of thepolynucleotide. In other words, the one or more modifications increasethe processivity of the Hel308 helicase by preventing dissociation fromthe polynucleotide strand. The thermal stability of the enzyme is alsoincreased by the one or more modifications giving it an improvedstructural stability that is beneficial in Strand Sequencing. Themodified Hel308 helicases of the invention have all of the advantagesand uses discussed above.

The modified Hel308 helicase has the ability to control the movement ofa polynucleotide. This can be measured as discussed above. The modifiedHel308 helicase is artificial or non-natural.

A modified Hel308 helicase of the invention may be isolated,substantially isolated, purified or substantially purified as discussedabove.

The Hel308 helicase preferably comprises a variant of one of thehelicases shown in Table 1 above which comprises one or more cysteineresidues and/or one or more non-natural amino acids at one or more ofthe positions which correspond to D272, N273, D274, G281, E284, E285,E287, S288, T289, G290, E291, D293, T294, N300, R303, K304, N314, S315,N316, H317, R318, K319, L320, E322, R326, N328, S615, K717, Y720, N721and S724 in Hel308 Mbu (SEQ ID NO: 10). The Hel308 helicase preferablycomprises a variant of one of SEQ ID NOs: 10, 13, 16, 19, 22, 25, 28,29, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50,51, 52, 53, 54, 55 and 58 which comprises one or more cysteine residuesand/or one or more non-natural amino acids at one or more of thepositions which correspond to D272, N273, D274, G281, E284, E285, E287,S288, T289, G290, E291, D293, T294, N300, R303, K304, N314, S315, N316,H317, R318, K319, L320, E322, R326, N328, S615, K717, Y720, N721 andS724 in Hel308 Mbu (SEQ ID NO: 10).

The Hel308 helicase preferably comprises a variant of one of SEQ ID NOs:10, 13, 16, 19, 22, 25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43,44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 and 58 which comprisesone or more cysteine residues and/or one or more non-natural amino acidsat one or more of the positions which correspond to D274, E284, E285,E287, S288, T289, G290, E291, N316, K319, S615, K717 or Y720 in Hel308Mbu (SEQ ID NO: 10).

Table 4a and 4b below show the positions in other Hel308 helicases whichcorrespond to D274, E284, E285, S288, S615, K717, Y720, E287, T289,G290, E291, N316 and K319 in Hel308 Mbu (SEQ ID NO: 10). For instance,in Hel308 Hvo (SEQ ID NO:16), E283 corresponds to D274 in Hel308 Mbu,E293 corresponds to E284 in Hel308 Mbu, 1294 corresponds to E285 inHel308 Mbu, V297 corresponds to S288 in Hel308 Mbu, D671 corresponds toS615 in Hel308 Mbu, K775 corresponds to K717 in Hel308 Mbu and E778corresponds to Y720 in Hel308 Mbu. The lack of a corresponding positionin another Hel308 helicase is marked as a “-”.

TABLE 4a Positions which correspond to D274, E284, E285, S288, S615,K717 and Y720 in Hel308 Mbu (SEQ ID NO: 10). SEQ Hel308 ID NO: homologueA B C D E F G 10 Mbu D274 E284 E285 S288 S615 K717 Y720 13 Pfu L265 E275L276 S279 P585 K690 E693 16 Hvo E283 E293 I294 V297 D671 K775 E778 19Hla E283 E293 I294 G297 D668 R775 E778 22 Csy D280 K290 I291 S294 P589T694 N697 25 Sso L281 K291 Q292 D295 D596 K702 Q705 28 Mfr H264 E272K273 A276 G576 K678 E681 29 Mok S279 L289 S290 D293 P649 K753 R756 32Mig Y276 L286 S287 D290 P579 K679 K682 33 Tga L266 S276 L277 Q280 P583K689 D692 34 Tba L287 E297 L298 S301 S604 K710 E713 37 Tsi L289 Q299L300 G303 N606 G712 E715 38 Mba E274 D284 E285 E288 S589 K691 D694 39Mac E274 D284 E285 E288 P590 K692 E695 40 Mmah H272 L282 S283 D286 P621K725 K728 41 Mmaz E274 D284 E285 E288 P590 K692 E698 42 Mth A269 L279A280 L283 H575 K677 E680 43 Mzh H274 Q284 E285 E288 P596 K699 Q702 44Mev G274 E284 E285 E288 T590 K691 Y694 45 Mma H272 L282 S283 D286 P621K725 K728 46 Nma G277 T287 E288 E291 D634 K737 E740 47 Mbo A270 E277R278 E281 S583 G685 E688 48 Fac Q264 F267 E268 E271 P559 K663 K666 49Mfe R275 L285 S286 E289 P576 K676 K679 50 Mja I273 L283 S284 E287 P574K674 K677 51 Min R257 L267 S268 D271 P554 K651 K654 52 Mhu S269 Q277E278 R281 S583 G685 R688 53 Afu K268 K277 A278 E281 D575 R677 E680 54Htu D277 D287 D288 D291 D626 K729 E732 55 Hpa D276 D286 Q287 D290 D595K707 E710 58 Hsp (ski2- E286 E296 I297 V300 D633 A737 E740 likehelicase)

TABLE 4b Positions which correspond to E287, T289, G290, E291, N316 andK319 in Hel308 Mbu (SEQ ID NO: 10). SEQ ID Hel308 NO: homologue H I J KL M 10 Mbu E287 T289 G290 E291 N316 K319 13 Pfu D278 L280 E281 E282 D307V310 16 Hvo D296 S298 D299 T300 E324 T327 19 Hla S296 S298 D299 T300E324 A327 22 Csy S293 G295 G296 E297 D322 S325 25 Sso D294 I296 E297E298 A325 D328 28 Mfr E275 A277 A278 E279 M304 T307 29 Mok L292 N294P295 T296 E320 K323 32 Mig L289 P291 P292 T293 E317 K320 33 Tga S279L281 E282 D283 V308 T311 34 Tba E300 L302 E303 S304 A329 T332 37 TsiD302 L304 D305 T306 T331 S334 38 Mba L287 N289 S290 E291 P316 E319 39Mac L287 N289 S290 E291 P316 E319 40 Mmah L285 R287 P288 V289 K313 K31641 Mmaz I287 N289 S290 E291 P316 E319 42 Mth R282 S284 G285 E286 E311R314 43 Mzh G287 A289 G290 E291 E316 R319 44 Mev L287 T289 S290 D291A316 K319 45 Mma L285 R287 P288 V289 K313 K316 46 Nma R290 D292 S293D294 T319 S322 47 Mbo L280 G282 T283 P284 K309 S312 48 Fac L270 I272P273 P274 D299 T302 49 Mfe L288 P290 P291 T292 Q316 K319 50 Mja L286P288 P289 T290 Q314 K317 51 Min F270 P272 P273 T274 E298 K301 52 MhuR280 L282 R283 D284 Q309 T312 53 Afu L280 E282 N283 E284 G309 R312 54Htu R290 D292 S293 D294 T319 S322 55 Hpa R289 V291 S292 D293 D318 S32158 Hsp (ski2- G299 S301 D302 T303 E327 E330 like helicase)

The Hel308 helicase more preferably comprises a variant of one of SEQ IDNOs: 10, 13, 16, 19, 22, 25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42,43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 and 58 whichcomprises one or more cysteine residues and/or one or more non-naturalamino acids at one or more of the positions which correspond to D274,E284, E285, S288, 5615, K717 and Y720 in Hel308 Mbu (SEQ ID NO: 10). Therelevant positions are shown in columns A to G in Table 4a above.

The helicase may comprise a cysteine residue at one, two, three, four,five, six or seven of the positions which correspond to D274, E284,E285, S288, S615, K717 and Y720 in Hel308 Mbu (SEQ ID NO: 10). Anycombination of these positions may be substituted with cysteine. Forinstance, for each row of Table 4a above, the helicase of the inventionmay comprise a cysteine at any of the following combinations of thepositions labelled A to G in that row: {A}, {B}, {C}, {D}, {G}, {E},{F}, {A and B}, {A and C}, {A and D}, {A and G}, {A and E}, {A and F},{B and C}, {B and D}, {B and G}, {B and E}, {B and F}, {C and D}, {C andG}, {C and E}, {C and F}, {D and G}, {D and E}, {D and F}, {G and E}, {Gand F}, {E and F}, {A, B and C}, {A, B and D}, {A, B and G}, {A, B andE}, {A, B and F}, {A, C and D}, {A, C and G}, {A, C and E}, {A, C andF}, {A, D and G}, {A, D and E}, {A, D and F}, {A, G and E}, {A, G andF}, {A, E and F}, {B, C and D}, {B, C and G}, {B, C and E}, {B, C andF}, {B, D and G}, {B, D and E}, {B, D and F}, {B, G and E}, {B, G andF}, {B, E and F}, {C, D and G}, {C, D and E}, {C, D and F}, {C, G andE}, {C, G and F}, {C, E and F}, {D, G and E}, {D, G and F}, {D, E andF}, {G, E and F}, {A, B, C and D}, {A, B, C and G}, {A, B, C and E}, {A,B, C and F}, {A, B, D and G}, {A, B, D and E}, {A, B, D and F}, {A, B, Gand E}, {A, B, G and F}, {A, B, E and F}, {A, C, D and G}, {A, C, D andE}, {A, C, D and F}, {A, C, G and E}, {A, C, G and F}, {A, C, E and F},{A, D, G and E}, {A, D, G and F}, {A, D, E and F}, {A, G, E and F}, {B,C, D and G}, {B, C, D and E}, {B, C, D and F}, {B, C, G and E}, {B, C, Gand F}, {B, C, E and F}, {B, D, G and E}, {B, D, G and F}, {B, D, E andF}, {B, G, E and F}, {C, D, G and E}, {C, D, G and F}, {C, D, E and F},{C, G, E and F}, {D, G, E and F}, {A, B, C, D and G}, {A, B, C, D andE}, {A, B, C, D and F}, {A, B, C, G and E}, {A, B, C, G and F}, {A, B,C, E and F}, {A, B, D, G and E}, {A, B, D, G and F}, {A, B, D, E and F},{A, B, G, E and F}, {A, C, D, G and E}, {A, C, D, G and F}, {A, C, D, Eand F}, {A, C, G, E and F}, {A, D, G, E and F}, {B, C, D, G and E}, {B,C, D, G and F}, {B, C, D, E and F}, {B, C, G, E and F}, {B, D, G, E andF}, {C, D, G, E and F}, {A, B, C, D, G and E}, {A, B, C, D, G and F},{A, B, C, D, E and F}, {A, B, C, G, E and F}, {A, B, D, G, E and F}, {A,C, D, G, E and F}, {B, C, D, G, E and F}, or {A, B, C, D, G, E and F}.

The helicase may comprises a non-natural amino acid, such as Faz, atone, two, three, four, five, six or seven of the positions whichcorrespond to D274, E284, E285, S288, S615, K717 and Y720 in Hel308 Mbu(SEQ ID NO: 10). Any combination of these positions may be substitutedwith a non-natural amino acid, such as Faz. For instance, for each rowof Table 4a above, the helicase of the invention may comprise anon-natural amino acid, such as Faz, at any of the combinations of thepositions labelled A to G above.

The helicase may comprise a combination of one or more cysteines and oneor more non-natural amino acids, such as Faz, at two or more of thepositions which correspond to D274, E284, E285, S288, 5615, K717 andY720 in Hel308 Mbu (SEQ ID NO: 10). Any combination of one or morecysteine residues and one or more non-natural amino acids, such as Faz,may be present at the relevant positions. For instance, for each row ofTable 4a and 4b above, the helicase of the invention may comprise one ormore cysteines and one or more non-natural amino acids, such as Faz, atany of the combinations of the positions labelled A to G above.

The Hel308 helicase more preferably comprises a variant of one of SEQ IDNOs: 10, 13, 16, 19, 22, 25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42,43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55 and 58 whichcomprises one or more cysteine residues and/or one or more non-naturalamino acids at one or more of the positions which correspond to D274,E284, E285, S288 and S615 in Hel308 Mbu (SEQ ID NO: 10). The relevantpositions are shown in columns A to E in Table 4a above.

The helicase may comprise a cysteine residue at one, two, three, four orfive, six or seven of the positions which correspond to D274, E284,E285, S288, S615, K717 and Y720 in Hel308 Mbu (SEQ ID NO: 10). Anycombination of these positions may be substituted with cysteine. Forinstance, for each row of Table 4a above, the helicase of the inventionmay comprise a cysteine at any of the following combinations of thepositions labelled A to E in that row: {A}, {B}, {C}, {D}, {E}, {A andB}, {A and C}, {A and D}, {A and E}, {B and C}, {B and D}, {B and E}, {Cand D}, {C and E}, {D and E}, {A, B and C}, {A, B and D}, {A, B and E},{A, C and D}, {A, C and E}, {A, D and E}, {B, C and D}, {B, C and E},{B, D and E}, {C, D and E}, {A, B, C and D}, {A, B, C and E}, {A, B, Dand E}, {A, C, D and E}, {B, C, D and E} or {A, B, C, D and E}.

The helicase may comprises a non-natural amino acid, such as Faz, atone, two, three, four or five of the positions which correspond to D274,E284, E285, S288, S615, K717 and Y720 in Hel308 Mbu (SEQ ID NO: 10). Anycombination of these positions may be substituted with a non-naturalamino acid, such as Faz. For instance, for each row of Table 4a above,the helicase of the invention may comprise a non-natural amino acid,such as Faz, at any of the combinations of the positions labelled A to Eabove.

The helicase may comprise a combination of one or more cysteines and oneor more non-natural amino acids, such as Faz, at two or more of thepositions which correspond to D274, E284, E285, S288 and S615 in Hel308Mbu (SEQ ID NO: 10). Any combination of one or more cysteine residuesand one or more non-natural amino acids, such as Faz, may be present atthe relevant positions. For instance, for each row of Table 4a above,the helicase of the invention may comprise one or more cysteines and oneor more non-natural amino acids, such as Faz, at any of the combinationsof the positions labelled A to E above.

The Hel308 helicase preferably comprises a variant of the sequence ofHel308 Mbu (i.e. SEQ ID NO: 10) which comprises one or more cysteineresidues and/or one or more non-natural amino acids at D272, N273, D274,G281, E284, E285, E287, S288, T289, G290, E291, D293, T294, N300, R303,K304, N314, 5315, N316, H317, R318, K319, L320, E322, R326, N328, S615,K717, Y720, N721 and S724. The variant preferably comprises D272C,N273C, D274C, G281C, E284C, E285C, E287C, S288C, T289C, G290C, E291C,D293C, T294C, N300C, R303C, K304C, N314C, S315C, N316C, H317C, R318C,K319C, L320C, E322C, R326C, N328C, S615C, K717C, Y720C, N721C or S724C.The variant preferably comprises D272Faz, N273Faz, D274Faz, G281Faz,E284Faz, E285Faz, E287Faz, S288Faz, T289Faz, G290Faz, E291Faz, D293Faz,T294Faz, N300Faz, R303Faz, K304Faz, N314Faz, S315Faz, N316Faz, H317 Faz,R318Faz, K319Faz, L320Faz, E322Faz, R326Faz, N328Faz, S615Faz, K717Faz,Y720Faz, N721Faz or S724Faz.

The Hel308 helicase preferably comprises a variant of the sequence ofHel308 Mbu (i.e. SEQ ID NO: 10) which comprises one or more cysteineresidues and/or one or more non-natural amino acids at D274, E284, E285,S288, S615, K717 and Y720. The helicase of the invention may compriseone or more cysteines, one or more non-natural amino acids, such as Faz,or a combination thereof at any of the combinations of the positionslabelled A to G above.

The Hel308 helicase preferably comprises a variant of the sequence ofHel308 Mbu (i.e. SEQ ID NO: 10) which comprises one or more cysteineresidues and/or one or more non-natural amino acids at one or more ofD274, E284, E285, S288 and S615. For instance, for Hel308 Mbu (SEQ IDNO: 10), the helicase of the invention may comprise a cysteine or anon-natural amino acid, such as Faz, at any of the followingcombinations of positions: {D274}, {E284}, {E285}, {S288}, {S615}, {D274and E284}, {D274 and E285}, {D274 and S288}, {D274 and S615}, {E284 andE285}, {E284 and S288}, {E284 and S615}, {E285 and S288}, {E285 andS615}, {S288 and S615}, {D274, E284 and E285}, {D274, E284 and S288},{D274, E284 and S615}, {D274, E285 and S288}, {D274, E285 and S615},{D274, S288 and S615}, {E284, E285 and S288}, {E284, E285 and S615},{E284, S288 and S615}, {E285, S288 and S615}, {D274, E284, E285 andS288}, {D274, E284, E285 and S615}, {D274, E284, S288 and S615}, {D274,E285, S288 and 5615}, E284, E285, S288 and S6151 or {D274, E284, E285,S288 and S615}.

The helicase preferably comprises a variant of SEQ ID NO: 10 whichcomprises (a) E284C and S615C, (b), E284Faz and S615Faz, (c) E284C andS615Faz or (d) E284Faz and S615C.

The helicase more preferably comprises the sequence shown in SEQ ID NO:10 with E284C and S615C.

Preferred non-natural amino acids for use in the invention include, butare not limited, to 4-Azido-L-phenylalanine (Faz),4-Acetyl-L-phenylalanine, 3-Acetyl-L-phenylalanine,4-Acetoacetyl-L-phenylalanine, O-Allyl-L-tyrosine,3-(Phenylselanyl)-L-alanine, O-2-Propyn-1-yl-L-tyrosine,4-(Dihydroxyboryl)-L-phenylalanine,4-[(Ethylsulfanyl)carbonyl]-L-phenylalanine,(2S)-2-amino-3-{4-[(propan-2-ylsulfanyl)carbonyl]phenyl}propanoic acid,(25)-2-amino-3-{4-[(2-amino-3-sulfanylpropanoyl)amino]phenyl}propanoicacid, O-Methyl-L-tyrosine, 4-Amino-L-phenylalanine,4-Cyano-L-phenylalanine, 3-Cyano-L-phenylalanine,4-Fluoro-L-phenylalanine, 4-Iodo-L-phenylalanine,4-Bromo-L-phenylalanine, O-(Trifluoromethyl)tyrosine,4-Nitro-L-phenylalanine, 3-Hydroxy-L-tyrosine, 3-Amino-L-tyrosine,3-Iodo-L-tyrosine, 4-Isopropyl-L-phenylalanine,3-(2-Naphthyl)-L-alanine, 4-Phenyl-L-phenylalanine,(2S)-2-amino-3-(naphthalen-2-ylamino)propanoic acid,6-(Methylsulfanyl)norleucine, 6-Oxo-L-lysine, D-tyrosine,(2R)-2-Hydroxy-3-(4-hydroxyphenyl)propanoic acid,(2R)-2-Ammoniooctanoate3-(2,2′-Bipyridin-5-yl)-D-alanine,2-amino-3-(8-hydroxy-3-quinolyl)propanoic acid,4-Benzoyl-L-phenylalanine, S-(2-Nitrobenzyl)cysteine,(2R)-2-amino-3-[(2-nitrobenzyl)sulfanyl]propanoic acid,(2S)-2-amino-3-[(2-nitrobenzyl)oxy]propanoic acid,O-(4,5-Dimethoxy-2-nitrobenzyl)-L-serine,(2S)-2-amino-6-({[(2-nitrobenzyl)oxy]carbonyl}amino)hexanoic acid,O-(2-Nitrobenzyl)-L-tyrosine, 2-Nitrophenylalanine,4-[(E)-Phenyldiazenyl]-L-phenylalanine,4-[3-(Trifluoromethyl)-3H-diaziren-3-yl]-D-phenylalanine,2-amino-3-[[5-(dimethylamino)-1-naphthyl]sulfonylamino]propanoic acid,(2S)-2-amino-4-(7-hydroxy-2-oxo-2H-chromen-4-yl)butanoic acid,(2S)-3-[(6-acetylnaphthalen-2-yl)amino]-2-aminopropanoic acid,4-(Carboxymethyl)phenylalanine, 3-Nitro-L-tyrosine, O-Sulfo-L-tyrosine,(2R)-6-Acetamido-2-ammoniohexanoate, 1-Methylhistidine, 2-Aminononanoicacid, 2-Aminodecanoic acid, L-Homocysteine, 5-Sulfanylnorvaline,6-Sulfanyl-L-norleucine, 5-(Methylsulfanyl)-L-norvaline,N⁶-{[(2R,3R)-3-Methyl-3,4-dihydro-2H-pyrrol-2-yl]carbonyl}-L-lysine,N⁶-[(Benzyloxy)carbonyl]lysine,(2S)-2-amino-6-[(cyclopentylcarbonyl)amino]hexanoic acid,N⁶-[(Cyclopentyloxy)carbonyl]-L-lysine,(2S)-2-amino-6-{[(2R)-tetrahydrofuran-2-ylcarbonyl]amino}hexanoic acid,(2S)-2-amino-8-[(2R,3S)-3-ethynyltetrahydrofuran-2-yl]-8-oxooctanoicacid, N⁶-(tert-Butoxycarbonyl)-L-lysine,(2S)-2-Hydroxy-6-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)hexanoicacid, N⁶-[(Allyloxy)carbonyl]lysine,(2S)-2-amino-6-({[(2-azidobenzyl)oxy]carbonyl}amino)hexanoic acid,N⁶-L-Prolyl-L-lysine,(2S)-2-amino-6-{[(prop-2-yn-1-yloxy)carbonyl]amino}hexanoic acid andN⁶-[(2-Azidoethoxy)carbonyl]-L-lysine.

The most preferred non-natural amino acid is 4-azido-L-phenylalanine(Faz).

As discussed above, variant of a Hel308 helicase is an enzyme that hasan amino acid sequence which varies from that of the wild-type helicaseand which retains polynucleotide binding activity. In the Hel308helicases of the invention, a variant of one of SEQ ID NOs: 10, 13, 16,19, 22, 25, 28, 29, 32, 33, 34, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46,47, 48, 49, 50, 51, 52, 53, 54, 55 and 58 may comprise additionalmodifications as long as it comprises one or more cysteine residuesand/or one or more non-natural amino acids at one or more of thepositions which correspond to D272, N273, D274, G281, E284, E285, E287,5288, T289, G290, E291, D293, T294, N300, R303, K304, N314, S315, N316,H317, R318, K319, L320, E322, R326, N328, S615, K717, Y720, N721 andS724 in Hel308 Mbu (SEQ ID NO: 10). Suitable modifications and variantsare discussed above with reference to the embodiments with two or moreparts connected.

A variant may comprise the mutations in domain 5 disclosed in Woodman etal. (J. Mol. Biol. (2007) 374, 1139-1144). These mutations correspond toR685A, R687A and R689A in SEQ ID NO: 10.

Connecting Two or More Parts of the Hel308 Helicases of the Invention

The Hel308 helicases modified in the invention comprise a polynucleotidebinding domain. Polynucleotide binding domains are defined above. Thepolynucleotide binding domain of an unmodified Hel308 helicase for usein the invention comprises an opening through which a polynucleotide canunbind from the helicase.

In a preferred embodiment, the Hel308 helicase is further modified suchthat two or more parts of the helicase are connected to reduce the sizeof an opening in the polynucleotide binding domain through which apolynucleotide can unbind from the helicase. The two or more parts maybe connected in any of the ways discussed above.

No Connection

In another embodiment, the Hel308 helicase is not modified such that twoor more parts of the helicase are connected to reduce the size of anopening in the polynucleotide binding domain through which apolynucleotide can unbind from the helicase. Preferably, none of the oneor more cysteines or one or more non-natural amino acids is connected toanother amino acid in the helicase. Preferably, no two amino acids inthe helicase are connected together via their natural or non-natural Rgroups.

Construct

The invention also provides a construct comprising a helicase of theinvention and an additional polynucleotide binding moiety, wherein thehelicase is attached to the polynucleotide binding moiety and theconstruct has the ability to control the movement of a polynucleotide.The helicase is attached to the additional polynucleotide bindingmoiety. The construct is artificial or non-natural.

A construct of the invention is a useful tool for controlling themovement of a polynucleotide during Strand Sequencing. A construct ofthe invention is even less likely than a modified helicase of theinvention to disengage from the polynucleotide being sequenced. Theconstruct can provide even greater read lengths of the polynucleotide asit controls the translocation of the polynucleotide through a nanopore.

A targeted construct that binds to a specific polynucleotide sequencecan also be designed. As discussed in more detail below, thepolynucleotide binding moiety may bind to a specific polynucleotidesequence and thereby target the helicase portion of the construct to thespecific sequence.

The construct has the ability to control the movement of apolynucleotide. This can be determined as discussed above.

A construct of the invention may be isolated, substantially isolated,purified or substantially purified. A construct is isolated or purifiedif it is completely free of any other components, such as lipids,polynucleotides or pore monomers. A construct is substantially isolatedif it is mixed with carriers or diluents which will not interfere withits intended use. For instance, a construct is substantially isolated orsubstantially purified if it is present in a form that comprises lessthan 10%, less than 5%, less than 2% or less than 1% of othercomponents, such as lipids, polynucleotides or pore monomers.

The helicase is preferably covalently attached to the additionalpolynucleotide binding moiety. The helicase may be attached to themoiety at more than one, such as two or three, points.

The helicase can be covalently attached to the moiety using any methodknown in the art. Suitable methods are discussed above with reference toconnecting the two or more parts.

The helicase and moiety may be produced separately and then attachedtogether. The two components may be attached in any configuration. Forinstance, they may be attached via their terminal (i.e. amino or carboxyterminal) amino acids. Suitable configurations include, but are notlimited to, the amino terminus of the moiety being attached to thecarboxy terminus of the helicase and vice versa. Alternatively, the twocomponents may be attached via amino acids within their sequences. Forinstance, the moiety may be attached to one or more amino acids in aloop region of the helicase. In a preferred embodiment, terminal aminoacids of the moiety are attached to one or more amino acids in the loopregion of a helicase.

In a preferred embodiment, the helicase is chemically attached to themoiety, for instance via one or more linker molecules as discussedabove. In another preferred embodiment, the helicase is geneticallyfused to the moiety. A helicase is genetically fused to a moiety if thewhole construct is expressed from a single polynucleotide sequence. Thecoding sequences of the helicase and moiety may be combined in any wayto form a single polynucleotide sequence encoding the construct. Geneticfusion of a pore to a nucleic acid binding protein is discussed inInternational Application No. PCT/GB09/001679 (published as WO2010/004265).

The helicase and moiety may be genetically fused in any configuration.The helicase and moiety may be fused via their terminal amino acids. Forinstance, the amino terminus of the moiety may be fused to the carboxyterminus of the helicase and vice versa. The amino acid sequence of themoiety is preferably added in frame into the amino acid sequence of thehelicase. In other words, the moiety is preferably inserted within thesequence of the helicase. In such embodiments, the helicase and moietyare typically attached at two points, i.e. via the amino and carboxyterminal amino acids of the moiety. If the moiety is inserted within thesequence of the helicase, it is preferred that the amino and carboxyterminal amino acids of the moiety are in close proximity and are eachattached to adjacent amino acids in the sequence of the helicase orvariant thereof. In a preferred embodiment, the moiety is inserted intoa loop region of the helicase.

The construct retains the ability of the helicase to control themovement of a polynucleotide. This ability of the helicase is typicallyprovided by its three dimensional structure that is typically providedby its β-strands and α-helices. The α-helices and β-strands aretypically connected by loop regions. In order to avoid affecting theability of the helicase to control the movement of a polynucleotide, themoiety is preferably genetically fused to either end of the helicase orinserted into a surface-exposed loop region of the helicase. The loopregions of specific helicases can be identified using methods known inthe art. In the Hel308 embodiments of the invention, the moiety ispreferably not genetically fused to any of the α-helixes.

The helicase may be attached directly to the moiety. The helicase ispreferably attached to the moiety using one or more, such as two orthree, linkers as discussed above. The one or more linkers may bedesigned to constrain the mobility of the moiety. The helicase and/orthe moiety may be modified to facilitate attachment of the one or morelinker as discussed above.

Cleavable linkers can be used as an aid to separation of constructs fromnon-attached components and can be used to further control the synthesisreaction. For example, a hetero-bifunctional linker may react with thehelicase, but not the moiety. If the free end of the linker can be usedto bind the helicase protein to a surface, the unreacted helicases fromthe first reaction can be removed from the mixture. Subsequently, thelinker can be cleaved to expose a group that reacts with the moiety. Inaddition, by following this sequence of linkage reactions, conditionsmay be optimised first for the reaction to the helicase, then for thereaction to the moiety after cleavage of the linker. The second reactionwould also be much more directed towards the correct site of reactionwith the moiety because the linker would be confined to the region towhich it is already attached.

The helicase may be covalently attached to the bifunctional crosslinkerbefore the helicase/crosslinker complex is covalently attached to themoiety. Alternatively, the moiety may be covalently attached to thebifunctional crosslinker before the bifunctional crosslinker/moietycomplex is attached to the helicase. The helicase and moiety may becovalently attached to the chemical crosslinker at the same time.

Preferred methods of attaching the helicase to the moiety are cysteinelinkage and Faz linkage as described above. In a preferred embodiment, areactive cysteine is presented on a peptide linker that is geneticallyattached to the moiety. This means that additional modifications willnot necessarily be needed to remove other accessible cysteine residuesfrom the moiety.

Cross-linkage of helicases or moieties to themselves may be prevented bykeeping the concentration of linker in a vast excess of the helicaseand/or moiety. Alternatively, a “lock and key” arrangement may be usedin which two linkers are used. Only one end of each linker may reacttogether to form a longer linker and the other ends of the linker eachreact with a different part of the construct (i.e. helicase or moiety).This is discussed in more detail below.

The site of attachment is selected such that, when the construct iscontacted with a polynucleotide, both the helicase and the moiety canbind to the polynucleotide and control its movement.

Attachment can be facilitated using the polynucleotide bindingactivities of the helicase and the moiety. For instance, complementarypolynucleotides can be used to bring the helicase and moiety together asthey hybridize. The helicase can be bound to one polynucleotide and themoiety can be bound to the complementary polynucleotide. The twopolynucleotides can then be allowed to hybridise to each other. Thiswill bring the helicase into close contact with the moiety, making thelinking reaction more efficient. This is especially helpful forattaching two or more helicases in the correct orientation forcontrolling movement of a target polynucleotide. An example ofcomplementary polynucleotides that may be used are shown below.

For helicase-Phi29 constructs the DNA below could be used.

Tags can be added to the construct to make purification of the constructeasier. These tags can then be chemically or enzymatically cleaved off,if their removal is necessary. Fluorophores or chromophores can also beincluded, and these could also be cleavable.

A simple way to purify the construct is to include a differentpurification tag on each protein (i.e. the helicase and the moiety),such as a hexa-His-tag and a Strep-tag®. If the two proteins aredifferent from one another, this method is particularly useful. The useof two tags enables only the species with both tags to be purifiedeasily.

If the two proteins do not have two different tags, other methods may beused. For instance, proteins with free surface cysteines or proteinswith linkers attached that have not reacted to form a construct could beremoved, for instance using an iodoacetamide resin for maleimidelinkers.

Constructs of the invention can also be purified from unreacted proteinson the basis of a different DNA processivity property. In particular, aconstruct of the invention can be purified from unreacted proteins onthe basis of an increased affinity for a polynucleotide, a reducedlikelihood of disengaging from a polynucleotide once bound and/or anincreased read length of a polynucleotide as it controls thetranslocation of the polynucleotide through a nanopore

A targeted construct that binds to a specific polynucleotide sequencecan also be designed. As discussed in more detail below, thepolynucleotide binding moiety may bind to a specific polynucleotidesequence and thereby target the helicase portion of the construct to thespecific sequence.

Polynucleotide Binding Moiety

The constructs of the invention comprise a polynucleotide bindingmoiety. A polynucleotide binding moiety is a polypeptide that is capableof binding to a polynucleotide. The moiety is preferably capable ofspecific binding to a defined polynucleotide sequence. In other words,the moiety preferably binds to a specific polynucleotide sequence, butdisplays at least 10 fold less binding to different sequences or morepreferably at least 100 fold less binding to different sequences or mostpreferably at least 1000 fold less binding to different sequences. Thedifferent sequence may be a random sequence. In some embodiments, themoiety binds to a specific polynucleotide sequence, but binding todifferent sequences cannot be measured. Moieties that bind to specificsequences can be used to design constructs that are targeted to suchsequences.

The moiety typically interacts with and modifies at least one propertyof a polynucleotide. The moiety may modify the polynucleotide bycleaving it to form individual nucleotides or shorter chains ofnucleotides, such as di- or trinucleotides. The moiety may modify thepolynucleotide by orienting it or moving it to a specific position, i.e.controlling its movement.

A polynucleotide, such as a nucleic acid, is a macromolecule comprisingtwo or more nucleotides. The polynucleotide or nucleic acid may compriseany combination of any nucleotides. The nucleotides can be naturallyoccurring or artificial. One or more nucleotides in the targetpolynucleotide can be oxidized or methylated. One or more nucleotides inthe target polynucleotide may be damaged. For instance, thepolynucleotide may comprise a pyrimidine dimer. Such dimers aretypically associated with damage by ultraviolet light and are theprimary cause of skin melanomas. One or more nucleotides in the targetpolynucleotide may be modified, for instance with a label or a tag.Suitable labels are described above. The target polynucleotide maycomprise one or more spacers.

A nucleotide typically contains a nucleobase, a sugar and at least onephosphate group. The nucleobase is typically heterocyclic. Nucleobasesinclude, but are not limited to, purines and pyrimidines and morespecifically adenine, guanine, thymine, uracil and cytosine. The sugaris typically a pentose sugar. Nucleotide sugars include, but are notlimited to, ribose and deoxyribose. The nucleotide is typically aribonucleotide or deoxyribonucleotide. The nucleotide typically containsa monophosphate, diphosphate or triphosphate. Phosphates may be attachedon the 5′ or 3′ side of a nucleotide.

Nucleotides include, but are not limited to, adenosine monophosphate(AMP), guanosine monophosphate (GMP), thymidine monophosphate (TMP),uridine monophosphate (UMP), cytidine monophosphate (CMP),5-methylcytidine monophosphate, 5-methylcytidine diphosphate,5-methylcytidine triphosphate, 5-hydroxymethylcytidine monophosphate,5-hydroxymethylcytidine diphosphate, 5-hydroxymethylcytidinetriphosphate cyclic adenosine monophosphate (cAMP), cyclic guanosinemonophosphate (cGMP), deoxyadenosine monophosphate (dAMP),deoxyguanosine monophosphate (dGMP), deoxythymidine monophosphate(dTMP), deoxyuridine monophosphate (dUMP) and deoxycytidinemonophosphate (dCMIP). The nucleotides are preferably selected from AMP,TMP, GMP, CMP, UMP, dAMP, dTMP, dGMP, dCMP and dUMP.

A nucleotide may be abasic (i.e. lack a nucleobase). A nucleotide mayalso lack a nucleobase and a sugar (i.e. is a C3 spacer).

The nucleotides in the polynucleotide may be attached to each other inany manner. The nucleotides are typically attached by their sugar andphosphate groups as in nucleic acids. The nucleotides may be connectedvia their nucleobases as in pyrimidine dimers.

The polynucleotide may be single stranded or double stranded. At least aportion of the polynucleotide is preferably double stranded.

The polynucleotide can be a nucleic acid, such as deoxyribonucleic acid(DNA) or ribonucleic acid (RNA). The target polynucleotide can compriseone strand of RNA hybridized to one strand of DNA. The polynucleotidemay be any synthetic nucleic acid known in the art, such as peptidenucleic acid (PNA), glycerol nucleic acid (GNA), threose nucleic acid(TNA), locked nucleic acid (LNA) or other synthetic polymers withnucleotide side chains.

It is preferred that the tertiary structure of the moiety is known.Knowledge of the three dimensional structure of the moiety allowsmodifications to be made to the moiety to facilitate its function in theconstruct of the invention.

The moiety may be any size and have any structure. For instance, themoiety may be an oligomer, such as a dimer or trimer. The moiety ispreferably a small, globular polypeptide formed from one monomer. Suchmoieties are easy to handle and are less likely to interfere with theability of the helicase to control the movement of the polynucleotide,particularly if fused to or inserted into the sequence of the helicase.

The amino and carboxy terminii of the moiety are preferably in closeproximity. The amino and carboxy terminii of the moiety are morepreferably presented on same face of the moiety. Such embodimentsfacilitate insertion of the moiety into the sequence of the helicase.For instance, if the amino and carboxy terminii of the moiety are inclose proximity, each can be attached by genetic fusion to adjacentamino acids in the sequence of the helicase.

It is also preferred that the location and function of the active siteof the moiety is known. This prevents modifications being made to theactive site that abolish the activity of the moiety. It also allows themoiety to be attached to the helicase so that the moiety binds to thepolynucleotide and controls its movement. Knowledge of the way in whicha moiety may bind to and orient polynucleotides also allows an effectiveconstruct to be designed.

The constructs of the invention are useful in Strand Sequencing. Themoiety preferably binds the polynucleotide in a buffer background whichis compatible with Strand Sequencing and the discrimination of thenucleotides. The moiety preferably has at least residual activity in asalt concentration well above the normal physiological level, such asfrom 100 mM to 2M. The moiety is more preferably modified to increaseits activity at high salt concentrations. The moiety may also bemodified to improve its processivity, stability and shelf life.

Suitable modifications can be determined from the characterisation ofpolynucleotide binding moieties from extremphiles such as halophilic,moderately halophilic bacteria, thermophilic and moderately thermophilicorganisms, as well as directed evolution approaches to altering the salttolerance, stability and temperature dependence of mesophilic orthermophilic exonucleases.

The polynucleotide binding moiety preferably comprises one or moredomains independently selected from helix-hairpin-helix (HhH) domains,eukaryotic single-stranded binding proteins (SSBs), bacterial SSBs,archaeal SSBs, viral SSBs, double-stranded binding proteins, slidingclamps, processivity factors, DNA binding loops, replication initiationproteins, telomere binding proteins, repressors, zinc fingers andproliferating cell nuclear antigens (PCNAs).

The helix-hairpin-helix (HhH) domains are polypeptide motifs that bindDNA in a sequence non-specific manner. They have been shown to confersalt stability and processivity when fused to polymerases, as well asincreasing their thermal stability. Suitable domains include domain H(residues 696-751) and domain HI (residues 696-802) from Topoisomerase Vfrom Methanopyrus kandleri (SEQ ID NO: 129). As discussed below, thepolynucleotide binding moiety may be domains H-L of SEQ ID NO: 129 asshown in SEQ ID NO: 130. Topoisomerase V from Methanopyrus kandleri isan example of a double-stranded binding protein as discussed below.

The HhH domain preferably comprises the sequence shown in SEQ ID NO: 94or 107 or 108 or a variant thereof. This domain increases theprocessivity and the salt tolerance of a helicase when used in aconstruct of the invention. A variant of SEQ ID NO: 94 or 107 or 108 isa protein that has an amino acid sequence which varies from that of SEQID NO: 94 or 107 or 108 and which retains polynucleotide bindingactivity. This can be measured as described above. A variant typicallyhas at least 50% homology to SEQ ID NO: 94 or 107 or 108 based on aminoacid identity over its entire sequence (or any of the % homologiesdiscussed above in relation to helicases) and retains polynucleotidebinding activity. A variant may differ from SEQ ID NO: 94 or 107 or 108in any of the ways discussed above in relation to helicases or below inrelation to pores. A variant preferably comprises one or moresubstituted cysteine residues and/or one or more substituted Fazresidues to facilitate attachment to the helicase as discussed above.

SSBs bind single stranded DNA with high affinity in a sequencenon-specific manner. They exist in all domains of life in a variety offorms and bind DNA either as monomers or multimers. Using amino acidsequence alignment and logorithms (such as Hidden Markov models) SSBscan be classified according to their sequence homology. The Pfam family,PF00436, includes proteins that all show sequence similarity to knownSSBs. This group of SSBs can then be further classified according to theStructural Classification of Proteins (SCOP). SSBs fall into thefollowing lineage: Class; All beta proteins, Fold; OB-fold, Superfamily:Nucleic acid-binding proteins, Family; Single strand DNA-binding domain,SSB. Within this family SSBs can be classified according to subfamilies,with several type species often characterised within each subfamily.

The SSB may be from a eukaryote, such as from humans, mice, rats, fungi,protozoa or plants, from a prokaryote, such as bacteria and archaea, orfrom a virus.

Eukariotic SSBs are known as replication protein A (RPAs). In mostcases, they are hetero-trimers formed of different size units. Some ofthe larger units (e.g. RPA70 of Saccharomyces cerevisiae) are stable andbind ssDNA in monomeric form.

Bacterial SSBs bind DNA as stable homo-tetramers (e.g. E. coli,Mycobacterium smegmatis and Helicobacter pylori) or homo-dimers (e.g.Deinococcus radiodurans and Thermotoga maritima). The SSBs from archaealgenomes are considered to be related with eukaryotic RPAs. Few of them,such as the SSB encoded by the crenarchaeote Sulfolobus solfataricus,are homo-tetramers. The SSBs from most other species are closer relatedto the replication proteins from eukaryotes and are referred to as RPAs.In some of these species they have been shown to be monomeric(Methanococcus jannaschii and Methanothermobacter thermoautotrophicum).Still, other species of Archaea, including Archaeoglobus fulgidus andMethanococcoides burtonii, appear to each contain two open readingframes with sequence similarity to RPAs. There is no evidence at proteinlevel and no published data regarding their DNA binding capabilities oroligomeric state. However, the presence of twooligonucleotide/oligosaccharide (OB) folds in each of these genes (threeOB folds in the case of one of the M. burtonii ORFs) suggests that theyalso bind single stranded DNA.

Viral SSBs bind DNA as monomers. This, as well as their relatively smallsize renders them amenable to genetic fusion to other proteins, forinstance via a flexible peptide linker. Alternatively, the SSBs can beexpressed separately and attached to other proteins by chemical methods(e.g. cysteines, unnatural amino-acids). This is discussed in moredetail below.

The SSB is preferably either (i) an SSB comprising a carboxy-terminal(C-terminal) region which does not have a net negative charge or (ii) amodified SSB comprising one or more modifications in its C-terminalregion which decreases the net negative charge of the C-terminal region.Such SSBs do not block the transmembrane pore and therefore allowcharacterization of the target polynucleotide.

Examples of SSBs comprising a C-terminal region which does not have anet negative charge include, but are not limited to, the humanmitochondrial SSB (HsmtSSB; SEQ ID NO: 118, the human replicationprotein A 70 kDa subunit, the human replication protein A 14 kDasubunit, the telomere end binding protein alpha subunit from Oxytrichanova, the core domain of telomere end binding protein beta subunit fromOxytricha nova, the protection of telomeres protein 1 (Pot1) fromSchizosaccharomyces pombe, the human Pot1, the OB-fold domains of BRCA2from mouse or rat, the p5 protein from phi29 (SEQ ID NO: 119) or avariant of any of those proteins. A variant is a protein that has anamino acid sequence which varies from that of the wild-type protein andwhich retains single stranded polynucleotide binding activity.Polynucleotide binding activity can be determined using methods known inthe art (and as described above). For instance, the ability of a variantto bind a single stranded polynucleotide can be determined as describedin the Examples.

A variant of SEQ ID NO 118 or 119 typically has at least 50% homology toSEQ ID NO: 118 or 119 based on amino acid identity over its entiresequence (or any of the % homologies discussed above in relation tohelicases) and retains single stranded polynucleotide binding activity.A variant may differ from SEQ ID NO: 118 or 119 in any of the waysdiscussed above in relation to helicases. In particular, a variant mayhave one or more conservative substitutions as shown in Tables 8 and 9.

Examples of SSBs which require one or more modifications in theirC-terminal region to decrease the net negative charge include, but arenot limited to, the SSB of E. coli (EcoSSB; SEQ ID NO: 120, the SSB ofMycobacterium tuberculosis, the SSB of Deinococcus radiodurans, the SSBof Thermus thermophiles, the SSB from Sulfolobus solfataricus, the humanreplication protein A 32 kDa subunit (RPA32) fragment, the CDCl3 SSBfrom Saccharomyces cerevisiae, the Primosomal replication protein N(PriB) from E. coli, the PriB from Arabidopsis thaliana, thehypothetical protein At4g28440, the SSB from T4 (gp32; SEQ ID NO: 121),the SSB from RB69 (gp32; SEQ ID NO: 95), the SSB from T7 (gp2.5; SEQ IDNO: 96) or a variant of any of these proteins. Hence, the SSB used inthe method of the invention may be derived from any of these proteins.

In addition to the one or more modifications in the C-terminal region,the SSB used in the method may include additional modifications whichare outside the C-terminal region or do not decrease the net negativecharge of the C-terminal region. In other words, the SSB used in themethod of the invention is derived from a variant of a wild-typeprotein. A variant is a protein that has an amino acid sequence whichvaries from that of the wild-type protein and which retains singlestranded polynucleotide binding activity. Polynucleotide bindingactivity can be determined as discussed above.

The SSB used in the invention may be derived from a variant of SEQ IDNO: 95, 96, 120 or 121. In other words, a variant of SEQ ID NO: 95, 96,120 or 121 may be used as the starting point for the SSB used in theinvention, but the SSB actually used further includes one or moremodifications in its C-terminal region which decreases the net negativecharge of the C-terminal region. A variant of SEQ ID NO: 95, 96, 120 or121 typically has at least 50% homology to SEQ ID NO: 95, 96, 120 or 121based on amino acid identity over its entire sequence (or any of the %homologies discussed above in relation to helicases) and retains singlestranded polynucleotide binding activity. A variant may differ from SEQID NO: 95, 96, 120 or 121 in any of the ways discussed above in relationto helicases. In particular, a variant may have one or more conservativesubstitutions as shown in Tables 8 and 9.

It is straightforward to identify the C-terminal region of the SSB inaccordance with normal protein N to C nomenclature. The C-terminalregion of the SSB is preferably about the last third of the SSB at theC-terminal end, such as the last third of the SSB at the C-terminal end.The C-terminal region of the SSB is more preferably about the lastquarter, fifth or eighth of the SSB at the C-terminal end, such as thelast quarter, fifth or eighth of the SSB at the C-terminal end. The lastthird, quarter, fifth or eighth of the SSB may be measured in terms ofnumbers of amino acids or in terms of actual length of the primarystructure of the SSB protein. The length of the various amino acids inthe N to C direction are known in the art.

The C-terminal region is preferably from about the last 10 to about thelast 60 amino acids of the C-terminal end of the SSB. The C-terminalregion is more preferably about the last 15, about the last 20, aboutthe last 25, about the last 30, about the last 35, about the last 40,about the last 45, about the last 50 or about the last 55 amino acids ofthe C-terminal end of the SSB.

The C-terminal region typically comprises a glycine and/or proline richregion. This proline/glycine rich region gives the C-terminal regionflexibility and can be used to identify the C-terminal region.

Suitable modifications for decreasing the net negative charge aredisclosed in U.S. Provisional Application No. 61/673,457 (filed 19 Jul.2012), U.S. Provisional Application No. 61/774,688 (filed 8 Mar. 2013)and the International application being filed concurrently with thisapplication (Oxford Nanopore Ref: ONT IP 035). The SSB may be any of theSSBs disclosed in the US Provisional Applications and Internationalapplication.

The modified SSB most preferably comprises a sequence selected fromthose shown in SEQ ID NOs: 103, 104, 122 to 125.

Double-stranded binding proteins bind double stranded DNA with highaffinity. Suitable double-stranded binding proteins include, but are notlimited to Mutator S (MutS; NCBI Reference Sequence: NP_417213.1; SEQ IDNO: 140), Sso7d (Sufolobus solfataricus P2; NCBI Reference Sequence:NP_343889.1; SEQ ID NO: 141; Nucleic Acids Research, 2004, Vol 32, No.3, 1197-1207), Sso10b1 (NCBI Reference Sequence: NP_342446.1; SEQ ID NO:142), Sso10b2 (NCBI Reference Sequence: NP_342448.1; SEQ ID NO: 143),Tryptophan repressor (Trp repressor; NCBI Reference Sequence:NP_291006.1; SEQ ID NO: 144), Lambda repressor (NCBI Reference Sequence:NP_040628.1; SEQ ID NO: 145), Cren7 (NCBI Reference Sequence:NP_342459.1; SEQ ID NO: 146), major histone classes H1/H5, H2A, H2B, H3and H4 (NCBI Reference Sequence: NP_066403.2, SEQ ID NO: 147), dsbA(NCBI Reference Sequence: NP_049858.1; SEQ ID NO: 148), Rad51 (NCBIReference Sequence: NP_002866.2; SEQ ID NO: 149), sliding clamps andTopoisomerase V Mka (SEQ ID NO: 129) or a variant of any of theseproteins. A variant of SEQ ID NO: 129, 140, 141, 142, 143, 144, 145,146, 147, 148 or 149 typically has at least 50% homology to SEQ ID NO:129, 140, 141, 142, 143, 144, 145, 146, 147, 148 or 149 based on aminoacid identity over its entire sequence (or any of the % homologiesdiscussed above in relation to helicases) and retains single strandedpolynucleotide binding activity. A variant may differ from SEQ ID NO:129, 140, 141, 142, 143, 144, 145, 146, 147, 148 or 149 in any of theways discussed above in relation to helicases. In particular, a variantmay have one or more conservative substitutions as shown in Tables 8 and9. Most polymerases achieve processivity by interacting with slidingclamps. In general, these are multimeric proteins (homo-dimers orhomo-trimers) that encircle dsDNA. These sliding clamps requireaccessory proteins (clamp loaders) to assemble them around the DNA helixin an ATP-dependent process. They also do not contact DNA directly,acting as a topological tether. As sliding clamps interact with theircognate polymerases in a specific manner via a polymerase domain, thisfragment could be fused to the helicase in order to incite recruitmentof helicases onto the sliding clamp. This interaction could be furtherstabilized by the generation of a covalent bond (introduction ofcysteines or unnatural amino-acids).

Related to DNA sliding clamps, processivity factors are viral proteinsthat anchor their cognate polymerases to DNA, leading to a dramaticincrease in the length of the fragments generated. They can be monomeric(as is the case for UL42 from Herpes simplex virus 1) or multimeric(UL44 from Cytomegalovirus is a dimer), they do not form closed ringsaround the DNA strand and they contact DNA directly. UL42 has been shownto increase processivity without reducing the rate of its correspondingpolymerase, suggesting that it interacts with DNA in a different mode toSSBs. The UL42 preferably comprises the sequence shown in SEQ ID NO: 97or SEQ ID NO: 102 or a variant thereof. A variant of SEQ ID NO: 97 or102 is a protein that has an amino acid sequence which varies from thatof SEQ ID NO: 97 or 102 and which retains polynucleotide bindingactivity. This can be measured as described above. A variant typicallyhas at least 50% homology to SEQ ID NO: 97 or 102 based on amino acididentity over its entire sequence (or any of the % homologies discussedabove in relation to helicases) and retains polynucleotide bindingactivity. A variant may differ from SEQ ID NO: 97 or SEQ ID NO: 102 inany of the ways discussed above in relation to helicases or below inrelation to pores. A variant preferably comprises one or moresubstituted cysteine residues and/or one or more substituted Fazresidues to facilitate attachment to the helicase as discussed above.

Attaching UL42 to a helicase could be done via genetic fusion orchemical attachment (cysteines, unnatural amino-acids). As thepolymerase polypeptide that binds UL42 is visible in the crystalstructure, these 35 amino acids (residues 1200-1235) could be fused ontothe C-terminus of the helicase and the natural affinity between thispolypeptide and the processivity factor used to form a complex. Theinteraction could be stabilized by introducing a covalent interaction(cysteines or unnatural amino-acids). One option is to utilize a naturalUL42 cysteine (C300) that is located close to the polypeptideinteraction site and introduce a point mutation into the polymerasepolypeptide (e.g. L1234C).

A reported method of increasing polymerase processivity is by exploitingthe interaction between E. coli thioredoxin (Trx) and the thioredoxinbinding domain (TBD) of bacteriophage T7 DNA polymerase (residues258-333). The binding of Trx to TBD causes the polypeptide to changeconformation to one that binds DNA. TBD is believed to clamp down onto aDNA strand and limit the polymerase off-rate, thus increasingprocessivity. Chimeric polymerases have been made by transferring TBDonto a non-processive polymerase, resulting in 1000 fold increase inpolymerised fragment length. There were no attempts to attach TBD to anyother class of proteins, but a covalent link between TBD and Trx wasengineered and can be used to stabilise the interaction.

Some helicases use accessory proteins in-vivo to achieve processivity(e.g. cisA from phage Φx174 and geneII protein from phage M13 for E.coli Rep helicase). Some of these proteins have been shown to interactwith more than one helicase (e.g. MutL acts on both UvrD and Rep, thoughnot to the same extent). These proteins have intrinsic DNA bindingcapabilities, some of them recognizing a specific DNA sequence. Theability of some of these accessory proteins to covalently attachthemselves to a specific DNA sequence could also be used to create a setstarting point for the helicase activity.

The proteins that protect the ends of chromosomes bind to telomericssDNA sequences in a highly specific manner. This ability could eitherbe exploited as is or by using point mutations to abolish the sequencespecificity.

Small DNA binding motifs (such as helix-turn-helix) recognize specificDNA sequences. In the case of the bacteriophage 434 repressor, a 62residue fragment was engineered and shown to retain DNA bindingabilities and specificity.

An abundant motif in eukaryotic proteins, zinc fingers consist of around30 amino-acids that bind DNA in a specific manner. Typically each zincfinger recognizes only three DNA bases, but multiple fingers can belinked to obtain recognition of a longer sequence.

Proliferating cell nuclear antigens (PCNAs) form a very tight clamp(doughnut) which slides up and down the dsDNA or ssDNA. The PCNA fromcrenarchaeota is unique in being a hetero-trimer so it is possible tofunctionalise one subunit and retain activity. Its subunits are shown inSEQ ID NOs: 98, 99 and 100. The PCNA is preferably a trimer comprisingthe sequences shown in SEQ ID NOs: 98, 99 and 100 or variants thereof.PCNA sliding clamp (NCBI Reference Sequence: ZP_06863050.1; SEQ ID NO:150) forms a dimer. The PCNA is preferably a dimer comprising SEQ ID NO:150 or a variant thereof. A variant is a protein that has an amino acidsequence which varies from that of SEQ ID NO: 98, 99, 100 or 150 andwhich retains polynucleotide binding activity. This can be measured asdescribed above. A variant is typically a trimer comprising sequencesthat have at least 50% homology to SEQ ID NOs: 98, 99 and 100 or a dimercomprising sequences that have at least 50% homology to SEQ ID NO: 150based on amino acid identity over each entire sequence (or any of the %homologies discussed above in relation to helicases) and which retainspolynucleotide binding activity. A variant may comprise sequences whichdiffer from SEQ ID NO: 98, 99, 100 or 150 in any of the ways discussedabove in relation to helicases or below in relation to pores. A variantpreferably comprises one or more substituted cysteine residues and/orone or more substituted Faz residues to facilitate attachment to thehelicase as discussed above. In a preferred embodiment, subunits 1 and 2of the PCNA from crenarchaeota (i.e. SEQ ID NOs: 98 and 99 or variantsthereof) are attached, such as genetically fused, and the resultingprotein is attached to a helicase to form a construct of the invention.During use of the construct, subunit 3 (i.e. SEQ ID NO: 100 or a variantthereof) may be added to complete the PCNA clamp (or doughnut) once theconstruct has bound the polynucleotide. In a preferred embodiment, onemonomer of the PCNA sliding clamp (i.e. SEQ ID NO: 150 or a variantthereof) is attached, such as genetically fused, to a helicase to form aconstruct of the invention. During use of the construct, the secondmonomer (i.e. SEQ ID NO: 150 or a variant thereof) may be added tocomplete the PCNA clamp (or doughnut) once the construct has bound thepolynucleotide.

The polynucleotide binding motif may be selected from any of those shownin Table 5 below.

TABLE 5 Suitable polynucleotide binding motifs MW No. Name ClassOrganism Structure Sequence Functional form (Da) Notes 1 SSBEco ssbEscherichia 1QVC P0AGE0 homo-tetramer 18975 coli 1EYG 2 SSBBhe ssbBartonella 3LGJ, Q6G302 homo-tetramer 16737 structure only henselae 3PGZ3 SSBCbu ssb Coxiella 3TQY Q83EP4 homo-tetramer 17437 structure onlyburnetii 4 SSBTma ssb Thermathoga 1Z9F Q9WZ73 homo-dimer 16298 small,maritima thermostable, salt independent DNA binding 5 SSBHpy ssbHelicobacter 2VW9 O25841 homo-tetramer 20143 pylori 6 SSBDra ssbDeinococcus 1SE8 Q9RY51 homo-dimer 32722 radiodurans 7 SSBTaq ssbThermus 2FXQ Q9KH06 homo-dimer 30026 aquaticus 8 SSBMsm ssbMycobacterium 3A5U,1X3E Q9AFI5 homo-tetramer 17401 tetramer more _smegmatis stable than E.coli, binding less salt dependent 9 SSBSsossb/RPA Sulfolobus 1O7I Q97W73 homo-tetramer 16138 similarities withsolfataricus RPA 10 SSBMHsmt ssb Homo 3ULL Q04837 homo-tetramer 17260sapiens 11 SSBMle ssb Mycobacterium 3AFP P46390 homo-tetramer 17701leprae 12 gp32T4 ssb Bacteriophage 1GPC P03695 monomer 33506 Homo-dimerin T4 the absence of DNA, monomer when binding DNA. 13 gp32RB69 ssbBacteriophage 2A1K Q7Y265 monomer 33118 RB69 14 gp2.5T7 ssbBacteriophage 1JE5 P03696 monomer 25694 T7 15 UL42 processivity Herpes1DML P10226 monomer 51159 binds ssDNA factor virus 1 dsDNA, structureshows link with polymerase 16 UL44 processivity Herpes virus 5 1YYPP16790 homo-dimer 46233 forms C shaped factor (cytomegalovirus) clamp onDNA 17 pf8 processivity KSHV 3I2M Q77ZG5 homo-dimer 42378 factor 18RPAMja RPA Methanococcus 3DM3 Q58559 monomer 73842 contains 4 OBjannaschii folds. Structure of fragment 19 RPAMma RPA Methanococcus3E0E, Q6LVF9 monomer 71388 Core domain maripaludis 2K5V structure 20RPAMth RPA Methanothermobacter monomer 120000 Shown tothermoautotrophicus interact directly with Hel308. Sequence from paper.21 RPA70Sce RPA Saccharomyces 1YNX P22336 hetero-trimer 70348 unit hastwo OB cerevisiae folds and binds DNA 22 RPAMbu1 RPA MethanococcoidesQ12V72 ? 41227 three OB folds burtonii identified 23 RPAMbu2 RPAMethanococcoides Q12W96 ? 47082 two OB folds burtonii identified 24RPA70Hsa RPA Homo sapiens 1JMC P27694 hetero-trimer 68138 25 RPA14HsaRPA Homo sapiens 3KDF P35244 hetero-trimer 13569 in complex with RPA3226 gp45T4 sliding Bacteriophage 1CZD P04525 homo-trimer 24858 ring shapeclamp T4 threads DNA 27 BetaEco sliding E.coli 3BEP P0A988 homo-dimer40587 ring shape clamp threads DNA, may bind ssDNA in poket 28 PCNAScesliding Saccharomyces 1PLQ,3K4X P15873 homo-dimer 28916 ring shape clampcerevisiae threads DNA 29 PCNATko sliding Thermococcus 3LX1 Q5JF32homo-dimer 28239 clamp kodakaraensis 30 PCNAHvo sliding Haloferax 3IFVD0VWY8 homo-dimer 26672 clamp volcanii 31 PCNAPfu sliding Pyrococcus1GE8 O73947 homo-dimer 28005 clamp furiosus 32 PCNAMbu slidingMethanococcoides Q12U18 homo-dimer 27121 Inferred from clamp burtoniihomology 33 BetaMtu sliding Mycobacterium 3P16 Q50790 homo-dimer 42113clamp tuberculosis 34 BetaTma sliding Thermotoga 1VPK Q9WYA0 homo-dimer40948 clamp maritima 35 BetaSpy sliding Streptococcus 2AVT Q9EVR1homo-dimer 41867 clamp pyrogenes 36 gp45RB69 sliding Bacteriophage 1B77O80164 homo-trimer 25111 Structure shows clamp RB69 interaction withpolypeptide fom polymerase 37 p55Hsa DNA Homo sapiens 2G4C, Q9UHNmonomer 54911 interacts with binding (mitochondrial) 3IKL, specificprotein 3IKM polymerase 38 p55Dme domain DNA Drosophylla Q9VJV8 monomer41027 associates with binding melanogaster polymerase protein Gammaconferring salt tolerance, processivity and increased activity 39 p55XlaDNA Xenopus laevis Q9W6G7 monomer 52283 binding protein 40 RepDSaureplication Staphylococcus P08115 homo-dimer 37874 increases initiationaurcus processivity of protein PcrA, covalently and specifically linksDNA 41 G2P replication Enterobacteriaphage P69546 monomer 46168increases initiation 1 processivity of protein Rep, covalently andspecifically links DNA 42 MutLEco mismatch Escherichia coli 1BKN, P23367homo-dimer 67924 increases repair 1B62, processivity of protein 1B63UvrD (and Rep) 43 KuMtu DNA Mycobacterium O05866 homo-dimer 30904increases repair tuberculosis processivity of protein UvrD1. Structureavailable for human Ku 44 OnTEBP telomere Oxytricha nova- 1OTC P29549hetero-dimer 56082 Specific biding binding Alpha to 3′ end proteinT4G4T4G4. Alpha subunit may be enough Oxytricha nova- P16458 41446 Beta45 EcrTEBP telomere Euplotes crassus Q06183 monomer 53360 Homolog tobinding OnTEBP with no protein Beta subunit in 46 TteTEBP telomereTetrachymena Q23FB9 hetero-dimer 53073 Homolog to binding termophilaAlpha OnTEBP-Alpha protein Tetrachymena Q23FH0 54757 May be homologtermophila Beta to OnTEBP Beta 47 pot1Spo telomere SchizosaccharomycesO13988 monomer 64111 related to TEBP binding pombe proteins 48 Cdc13pScetelomere Saccharomyces C7GSV7 monomer 104936 specific binding bindingcerevisiae to telomeric proteins DNA 49 C1 repressor BacteriophageP16117 homo-dimer 10426 binds DNA 434 specifically as homo-dimer 50 LexArepressor Escherichia 1LEB P0A7C2 homo-dimer 22358 binds DNA colispecifically as homo-dimer

The polynucleotide binding moiety is preferably derived from apolynucleotide binding enzyme. A polynucleotide binding enzyme is apolypeptide that is capable of binding to a polynucleotide andinteracting with and modifying at least one property of thepolynucleotide. The enzyme may modify the polynucleotide by cleaving itto form individual nucleotides or shorter chains of nucleotides, such asdi- or trinucleotides. The enzyme may modify the polynucleotide byorienting it or moving it to a specific position. The polynucleotidebinding moiety does not need to display enzymatic activity as long as itis capable of binding the polynucleotide and controlling its movement.For instance, the moiety may be derived from an enzyme that has beenmodified to remove its enzymatic activity or may be used underconditions which prevent it from acting as an enzyme.

The polynucleotide binding moiety is preferably derived from anucleolytic enzyme. The enzyme is more preferably derived from a memberof any of the Enzyme Classification (EC) groups 3.1.11, 3.1.13, 3.1.14,3.1.15, 3.1.16, 3.1.21, 3.1.22, 3.1.25, 3.1.26, 3.1.27, 3.1.30 and3.1.31. The enzyme may be any of those disclosed in InternationalApplication No. PCT/GB10/000133 (published as WO 2010/086603).

Preferred enzymes are exonucleases, polymerases, helicases andtopoisomerases, such as gyrases. Suitable exonucleases include, but arenot limited to, exonuclease I from E. coli, exonuclease III enzyme fromE. coli, RecJ from T. thermophilus and bacteriophage lambda exonucleaseand variants thereof.

The polymerase is preferably a member of any of the MoietyClassification (EC) groups 2.7.7.6, 2.7.7.7, 2.7.7.19, 2.7.7.48 and2.7.7.49. The polymerase is preferably a DNA-dependent DNA polymerase,an RNA-dependent DNA polymerase, a DNA-dependent RNA polymerase or anRNA-dependent RNA polymerase. The polynucleotide binding moiety ispreferably derived from Phi29 DNA polymerase (SEQ ID NO: 101). Themoiety may comprise the sequence shown in SEQ ID NO: 101 or a variantthereof. A variant of SEQ ID NO: 101 is an enzyme that has an amino acidsequence which varies from that of SEQ ID NO: 101 and which retainspolynucleotide binding activity. This can be measured as describedabove. The variant may include modifications that facilitate binding ofthe polynucleotide and/or facilitate its activity at high saltconcentrations and/or room temperature.

Over the entire length of the amino acid sequence of SEQ ID NO: 101, avariant will preferably be at least 50% homologous to that sequencebased on amino acid identity. More preferably, the variant polypeptidemay be at least 55%, at least 60%, at least 65%, at least 70%, at least75%, at least 80%, at least 85%, at least 90% and more preferably atleast 95%, 97% or 99% homologous based on amino acid identity to theamino acid sequence of SEQ ID NO: 101 over the entire sequence. Theremay be at least 80%, for example at least 85%, 90% or 95%, amino acididentity over a stretch of 200 or more, for example 230, 250, 270 or 280or more, contiguous amino acids (“hard homology”). Homology isdetermined as described below. The variant may differ from the wild-typesequence in any of the ways discussed below with reference to SEQ IDNOs: 2 and 4.

The helicase may be any of those discussed above. Helicase dimers andmultimers are discussed in detail below. The polynucleotide bindingmoiety may be a polynucleotide binding domain derived from a helicase.For instance, the polynucleotide binding moiety preferably comprises thesequence shown in SEQ ID NOs: 105 or 106 or a variant thereof. A variantof SEQ ID NOs: 105 or 106 is a protein that has an amino acid sequencewhich varies from that of SEQ ID NOs: 105 or 106 and which retainspolynucleotide binding activity. This can be measured as describedabove. The variant may include modifications that facilitate binding ofthe polynucleotide and/or facilitate its activity at high saltconcentrations and/or room temperature.

Over the entire length of the amino acid sequence of SEQ ID NOs: 105 or106, a variant will preferably be at least 50% homologous to thatsequence based on amino acid identity. More preferably, the variantpolypeptide may be at least 55%, at least 60%, at least 65%, at least70%, at least 75%, at least 80%, at least 85%, at least 90% and morepreferably at least 95%, 97% or 99% homologous based on amino acididentity to the amino acid sequence of SEQ ID NOs: 105 or 106 over theentire sequence. There may be at least 80%, for example at least 85%,90% or 95%, amino acid identity over a stretch of 40 or more, forexample 50, 60, 70 or 80 or more, contiguous amino acids (“hardhomology”). Homology is determined as described below. The variant maydiffer from the wild-type sequence in any of the ways discussed belowwith reference to SEQ ID NOs: 2 and 4.

The topoisomerase is preferably a member of any of the MoietyClassification (EC) groups 5.99.1.2 and 5.99.1.3.

The polynucleotide binding moiety may be any of the enzymes discussedabove.

The moiety may be labelled with a revealing label. The label may be anyof those described above.

The moiety may be isolated from any moiety-producing organism, such asE. coli, T. thermophilus or bacteriophage, or made synthetically or byrecombinant means. For example, the moiety may be synthesized by invitro translation and transcription as described below. The moiety maybe produced in large scale following purification as described below.

Helicase Oligomers

As will be clear from the discussion above, the polynucleotide bindingmoiety is preferably derived from a helicase. For instance, it may be apolynucleotide domain from a helicase. The moiety more preferablycomprises one or more helicases. The helicases may be any of thosediscussed above, including the helicases of the invention. In suchembodiments, the constructs of the invention of course comprise two ormore helicases attached together where at least one of the helicases ismodified in accordance with the invention. The constructs may comprisetwo, three, four, five or more helicases. In other words, the constructsof the invention may comprise a helicase dimer, a helicase trimer, ahelicase tetramer, a helicase pentamer and the like.

The two or more helicases can be attached together in any orientation.Identical or similar helicases may be attached via the same amino acidposition or spatially proximate amino acid positions in each helicase.This is termed the “head-to-head” formation. Alternatively, identical orsimilar helicases may be attached via positions on opposite or differentsides of each helicase. This is termed the “head-to-tail” formation.Helicase trimers comprising three identical or similar helicases maycomprise both the head-to-head and head-to-tail formations.

The two or more helicases may be different from one another (i.e. theconstruct is a hetero-dimer, -trimer, -tetramer or -pentamer etc.). Forinstance, the constructs of the invention may comprise: (a) one or moreHel308 helicases and one or more XPD helicases; (b) one or more Hel308helicases and one or more RecD helicases; (c) one or more Hel308helicases and one or more TraI helicases; (d) one or more XPD helicasesand one or more RecD helicases; (e) one or more XPD helicases and one ormore TraI helicases; or (f) one or more RecD helicases and one or moreTraI helicases. The construct may comprise two different variants of thesame helicase. For instance, the construct may comprise two variants ofone of the helicases discussed above with one or more cysteine residuesor Faz residues introduced at different positions in each variant. Inthis instance, the helicases can be in a head-to-tail formation. In apreferred embodiment, a variant of SEQ ID NO: 10 comprising Q442C may beattached via cysteine linkage to a variant of SEQ ID NO: 10 comprisingQ557C. Cys mutants of Hel308Mbu can also be made into hetero-dimers ifnecessary. In this approach, two different Cys mutant pairs such asHel308Mbu-Q442C and Hel308Mbu-Q577C can be linked in head-to-tailfashion. Hetero-dimers can be formed in two possible ways. The firstinvolves the use of a homo-bifunctional linker as discussed above. Oneof the helicase variants can be modified with a large excess of linkerin such a way that one linker is attached to one molecule of theprotein. This linker modified variant can then be purified away fromunmodified proteins, possible homo-dimers and unreacted linkers to reactwith the other helicase variant. The resulting dimer can then bepurified away from other species.

The second involves the use of hetero-bifunctional linkers. For example,one of the helicase variants can be modified with a first PEG linkercontaining maleimide or iodoacetamide functional group at one end and acyclooctyne functional group (DIBO) at the other end. An example of thisis shown below:

The second helicase variant can be modified with a second PEG linkercontaining maleimide or iodoacetamide functional group at one end and anazide functional group at the other end. An example is show below:

The two helicase variants with two different linkers can then bepurified and clicked together (using copper free click chemistry) tomake a dimer. Copper free click chemistry has been used in theseapplications because of its desirable properties. For example, it isfast, clean and not poisonous towards proteins. However, other suitablebio-orthogonal chemistries include, but are not limited to, Staudingerchemistry, hydrazine or hydrazide/aldehyde or ketone reagents (HyNic+4FBchemistry, including all Solulink™ reagents), Diels-Alder reagent pairsand boronic acid/salicyhydroxamate reagents.

These two ways of linking two different variants of the same helicaseare also valid for any of the constructs discussed above in which thehelicase and the moiety are different from one another, such as dimersof two different helicases and a helicase-polymerase dimer.

Similar methodology may also be used for linking different Faz variants.One Faz variant (such as SEQ ID NO: 10 comprising Q442Faz) can bemodified with a large excess of linker in such a way that one linker isattached to one molecule of the protein. This linker modified Fazvariant can then be purified away from unmodified proteins, possiblehomo-dimers and unreacted linkers to react with the second Faz variant(such as SEQ ID NO: 10 comprising Q577Faz). The resulting dimer can thenbe purified away from other species.

Hetero-dimers can also be made by linking cysteine variants and Fazvariants of the same helicase or different helicases. For example, anyof the above cysteine variants (such as SEQ ID NO: 10 comprising Q442C)can be used to make dimers with any of the above Faz variants (such SEQID NO: 10 comprising Q577Faz). Hetero-bifunctional PEG linkers withmaleimide or iodoacetamide functionalities at one end and DBCOfunctionality at the other end can be used in this combination ofmutants. An example of such a linker is shown below(DBCO-PEG4-maleimide):

The length of the linker can be varied by changing the number of PEGunits between the two functional groups.

Helicase hetero-trimers can comprise three different types of helicasesselected from Hel308 helicases, XPD helicases, RecD helicases, TraIhelicases and variants thereof. The same is true for oligomerscomprising more than three helicases. The two or more helicases within aconstruct may be different variants of the same helicase, such asdifferent variants of SEQ ID NO: 10, 22, 33 or 52. The differentvariants may be modified at different positions to facilitate attachmentvia the different positions. The hetero-trimers may therefore be in ahead-to-tail and head-to-head formation.

The two or more helicases in the constructs of the invention may be thesame as one another (i.e. the construct is a homo-dimer, -trimer,-tetramer or -pentamer etc.) Homo-oligomers can comprise two or moreHel308 helicases, two or more XPD helicases, two or more RecD helicases,two or more TraI helicases or two or more of any of the variantsdiscussed above. In such embodiments, the helicases are preferablyattached using the same position in each helicase. The helicases aretherefore attached head-to-head. The helicases may be linked using acysteine residue or a Faz residue that has been substituted into thehelicases at the same position. Cysteine residues in identical helicasevariants can be linked using a homo-bifunctional linker containing thiolreactive groups such as maleimide or iodoacetamide. These functionalgroups can be at the end of a polyethyleneglycol (PEG) chain as in thefollowing example:

The length of the linker can be varied to suit the requiredapplications. For example, n can be 2, 3, 4, 8, 11, 12, 16 or more. PEGlinkers are suitable because they have favourable properties such aswater solubility. Other non PEG linkers can also be used in cysteinelinkage.

By using similar approaches, identical Faz variants can also be madeinto homo-dimers. Homo-bifunctional linkers with DIBO functional groupscan be used to link two molecules of the same Faz variant to makehomo-dimers using Cu²⁺ free click chemistry. An example of a linker isgiven below:

The length of the PEG linker can vary to include 2, 4, 8, 12, 16 or morePEG units. Such linkers can also be made to incorporate a florescent tagto ease quantifications. Such fluorescence tags can also be incorporatedinto Maleimide linkers.

The invention also provides a construct comprising a helicase of theinvention and an amino acid sequence comprising SEQ ID NO: 130 (H-Ldomains from Topoisomerase V from Methanopyrus kandleri; SEQ ID NO: 129)or a variant thereof having at least 80% homology to SEQ ID NO: 130based on amino acid identity over the entire sequence of SEQ ID NO: 130,wherein the helicase is attached to the amino acid sequence and theconstruct has the ability to control the movement of a polynucleotide.The helicase may be attached to the amino acid sequence in any of theways discussed above.

Preferred constructs of the invention are shown in the Table 6 below.Each row shows a preferred construct in which the helicase in theleft-hand column is attached to additional polynucleotide binding moietyin the right-hand column in accordance with the invention. If thepolynucleotide binding moiety in the right-hand column is a helicase, itmay also be a helicase of the invention.

Helicase of the invention Additional polynucleotide binding moietyHel308 helicase of the invention as defined Polymerase (preferably SEQID NO: 101 or a above (preferably SEQ ID NO: 10, 22, 33 or variantthereof as defined above) 52 or a variant thereof as defined above) TraIhelicase of the invention as defined above Polymerase (preferably SEQ IDNO: 101 or a (preferably SEQ ID NO: 85, 126, 134 and 138 variant thereofas defined above) or a variant thereof as defined above) Hel308 helicaseof the invention as defined Hel308 helicase as defined above (preferablyabove (preferably SEQ ID NO: 10, 22, 33 or SEQ ID NO: 10, 22, 33 or 52or a variant 52 or a variant thereof as defined above) thereof asdefined above) TraI helicase of the invention as defined above TraIhelicase as defined above (preferably SEQ (preferably SEQ ID NO: 85,126, 134 and 138 ID NO: 85, 126, 134 and 138 or a variant or a variantthereof as defined above) thereof as defined above) Hel308 helicase ofthe invention as defined TraI helicase as defined above (preferably SEQabove (preferably SEQ ID NO: 10, 22, 33 or ID NO: 85, 126, 134 and 138or a variant 52 or a variant thereof as defined above) thereof asdefined above) TraI helicase of the invention as defined above He1308helicase as defined above (preferably (preferably SEQ ID NO: 85, 126,134 and 138 SEQ ID NO: 10, 22, 33 or 52 or a variant or a variantthereof as defined above) thereof as defined above)

Polynucleotide Sequences

Any of the proteins described herein may be expressed using methodsknown in the art. Polynucleotide sequences may be isolated andreplicated using standard methods in the art. Chromosomal DNA may beextracted from a helicase producing organism, such as Methanococcoidesburtonii, and/or a SSB producing organism, such as E. coli. The geneencoding the sequence of interest may be amplified using PCR involvingspecific primers. The amplified sequences may then be incorporated intoa recombinant replicable vector such as a cloning vector. The vector maybe used to replicate the polynucleotide in a compatible host cell. Thuspolynucleotide sequences may be made by introducing a polynucleotideencoding the sequence of interest into a replicable vector, introducingthe vector into a compatible host cell, and growing the host cell underconditions which bring about replication of the vector. The vector maybe recovered from the host cell. Suitable host cells for cloning ofpolynucleotides are known in the art and described in more detail below.

The polynucleotide sequence may be cloned into a suitable expressionvector. In an expression vector, the polynucleotide sequence istypically operably linked to a control sequence which is capable ofproviding for the expression of the coding sequence by the host cell.Such expression vectors can be used to express a construct.

The term “operably linked” refers to a juxtaposition wherein thecomponents described are in a relationship permitting them to functionin their intended manner. A control sequence “operably linked” to acoding sequence is ligated in such a way that expression of the codingsequence is achieved under conditions compatible with the controlsequences. Multiple copies of the same or different polynucleotide maybe introduced into the vector.

The expression vector may then be introduced into a suitable host cell.Thus, a construct can be produced by inserting a polynucleotide sequenceencoding a construct into an expression vector, introducing the vectorinto a compatible bacterial host cell, and growing the host cell underconditions which bring about expression of the polynucleotide sequence.

The vectors may be for example, plasmid, virus or phage vectors providedwith an origin of replication, optionally a promoter for the expressionof the said polynucleotide sequence and optionally a regulator of thepromoter. The vectors may contain one or more selectable marker genes,for example an ampicillin resistance gene. Promoters and otherexpression regulation signals may be selected to be compatible with thehost cell for which the expression vector is designed. A T7, trc, lac,ara or λ_(L) promoter is typically used.

The host cell typically expresses the construct at a high level. Hostcells transformed with a polynucleotide sequence will be chosen to becompatible with the expression vector used to transform the cell. Thehost cell is typically bacterial and preferably E. coli. Any cell with aλ DE3 lysogen, for example C41 (DE3), BL21 (DE3), JM109 (DE3), B834(DE3), TUNER, Origami and Origami B, can express a vector comprising theT7 promoter.

Methods of the Invention

The invention provides a method of controlling the movement of a targetpolynucleotide. The method comprises contacting the targetpolynucleotide with a helicase of the invention or a construct of theinvention and thereby controlling the movement of the polynucleotide.The method is preferably carried out with a potential applied across thepore. As discussed in more detail below, the applied potential typicallyresults in the formation of a complex between the pore and the helicaseor construct. The applied potential may be a voltage potential.Alternatively, the applied potential may be a chemical potential. Anexample of this is using a salt gradient across an amphiphilic layer. Asalt gradient is disclosed in Holden et al., J Am Chem Soc. 2007 Jul.11; 129(27):8650-5.

The invention also provides a method of characterising a targetpolynucleotide. The method comprises (a) contacting the targetpolynucleotide with a transmembrane pore and a helicase of the inventionor a construct of the invention such that the helicase or constructcontrols the movement of the target polynucleotide through the pore. Themethod also comprises (b) taking one or more measurements as thepolynucleotide moves with respect to the pore wherein the measurementsare indicative of one or more characteristics of the targetpolynucleotide and thereby characterising the target polynucleotide.

Steps (a) and (b) are preferably carried out with a potential appliedacross the pore as discussed above. In some instances, the currentpassing through the pore as the polynucleotide moves with respect to thepore is used to determine the sequence of the target polynucleotide.This is Strand Sequencing.

The method of the invention is for characterising a targetpolynucleotide. A polynucleotide is defined above.

The whole or only part of the target polynucleotide may be characterisedusing this method. The target polynucleotide can be any length. Forexample, the polynucleotide can be at least 10, at least 50, at least100, at least 150, at least 200, at least 250, at least 300, at least400 or at least 500 nucleotide pairs in length. The polynucleotide canbe 1000 or more nucleotide pairs, 5000 or more nucleotide pairs inlength or 100000 or more nucleotide pairs in length.

The target polynucleotide is present in any suitable sample. Theinvention is typically carried out on a sample that is known to containor suspected to contain the target polynucleotide. Alternatively, theinvention may be carried out on a sample to confirm the identity of oneor more target polynucleotides whose presence in the sample is known orexpected.

The sample may be a biological sample. The invention may be carried outin vitro on a sample obtained from or extracted from any organism ormicroorganism. The organism or microorganism is typically archaeal,prokaryotic or eukaryotic and typically belongs to one of the fivekingdoms: plantae, animalia, fungi, monera and protista. The inventionmay be carried out in vitro on a sample obtained from or extracted fromany virus. The sample is preferably a fluid sample. The sample typicallycomprises a body fluid of the patient. The sample may be urine, lymph,saliva, mucus or amniotic fluid but is preferably blood, plasma orserum. Typically, the sample is human in origin, but alternatively itmay be from another mammal animal such as from commercially farmedanimals such as horses, cattle, sheep or pigs or may alternatively bepets such as cats or dogs. Alternatively a sample of plant origin istypically obtained from a commercial crop, such as a cereal, legume,fruit or vegetable, for example wheat, barley, oats, canola, maize,soya, rice, bananas, apples, tomatoes, potatoes, grapes, tobacco, beans,lentils, sugar cane, cocoa, cotton.

The sample may be a non-biological sample. The non-biological sample ispreferably a fluid sample. Examples of a non-biological sample includesurgical fluids, water such as drinking water, sea water or river water,and reagents for laboratory tests.

The sample is typically processed prior to being assayed, for example bycentrifugation or by passage through a membrane that filters outunwanted molecules or cells, such as red blood cells. The sample may bemeasured immediately upon being taken. The sample may also be typicallystored prior to assay, preferably below −70° C.

A transmembrane pore is a structure that crosses the membrane to somedegree. It permits hydrated ions driven by an applied potential to flowacross or within the membrane. The transmembrane pore typically crossesthe entire membrane so that hydrated ions may flow from one side of themembrane to the other side of the membrane. However, the transmembranepore does not have to cross the membrane. It may be closed at one end.For instance, the pore may be a well in the membrane along which or intowhich hydrated ions may flow.

Any transmembrane pore may be used in the invention. The pore may bebiological or artificial. Suitable pores include, but are not limitedto, protein pores, polynucleotide pores and solid state pores.

Any membrane may be used in accordance with the invention. Suitablemembranes are well-known in the art. The membrane is preferably anamphiphilic layer. An amphiphilic layer is a layer formed fromamphiphilic molecules, such as phospholipids, which have both at leastone hydrophilic portion and at least one lipophilic or hydrophobicportion. The amphiphilic molecules may be synthetic or naturallyoccurring. Non-naturally occurring amphiphiles and amphiphiles whichform a monolayer are known in the art and include, for example, 7s(Gonzalez-Perez et al., Langmuir, 2009, 25, 10447-10450). Blockcopolymers are polymeric materials in which two or more monomersub-units that are polymerized together to create a single polymerchain. Block copolymers typically have properties that are contributedby each monomer sub-unit. However, a block copolymer may have uniqueproperties that polymers formed from the individual sub-units do notpossess. Block copolymers can be engineered such that one of the monomersub-units is hydrophobic (i.e. lipophilic), whilst the other sub-unit(s)are hydrophilic whilst in aqueous media. In this case, the blockcopolymer may possess amphiphilic properties and may form a structurethat mimics a biological membrane. The block copolymer may be a diblock(consisting of two monomer sub-units), but may also be constructed frommore than two monomer sub-units to form more complex arrangements thatbehave as amphipiles. The copolymer may be a triblock, tetrablock orpentablock copolymer.

The amphiphilic layer may be a monolayer or a bilayer. The amphiphiliclayer is typically a planar lipid bilayer or a supported bilayer.

The amphiphilic layer is typically a lipid bilayer. Lipid bilayers aremodels of cell membranes and serve as excellent platforms for a range ofexperimental studies. For example, lipid bilayers can be used for invitro investigation of membrane proteins by single-channel recording.Alternatively, lipid bilayers can be used as biosensors to detect thepresence of a range of substances. The lipid bilayer may be any lipidbilayer. Suitable lipid bilayers include, but are not limited to, aplanar lipid bilayer, a supported bilayer or a liposome. The lipidbilayer is preferably a planar lipid bilayer. Suitable lipid bilayersare disclosed in International Application No. PCT/GB08/000563(published as WO 2008/102121), International Application No.PCT/GB08/004127 (published as WO 2009/077734) and InternationalApplication No. PCT/GB2006/001057 (published as WO 2006/100484).

Methods for forming lipid bilayers are known in the art. Suitablemethods are disclosed in the Example. Lipid bilayers are commonly formedby the method of Montal and Mueller (Proc. Natl. Acad. Sci. USA., 1972;69: 3561-3566), in which a lipid monolayer is carried on aqueoussolution/air interface past either side of an aperture which isperpendicular to that interface.

The method of Montal & Mueller is popular because it is a cost-effectiveand relatively straightforward method of forming good quality lipidbilayers that are suitable for protein pore insertion. Other commonmethods of bilayer formation include tip-dipping, painting bilayers andpatch-clamping of liposome bilayers.

In a preferred embodiment, the lipid bilayer is formed as described inInternational Application No. PCT/GB08/004127 (published as WO2009/077734).

In another preferred embodiment, the membrane is a solid state layer. Asolid-state layer is not of biological origin. In other words, a solidstate layer is not derived from or isolated from a biologicalenvironment such as an organism or cell, or a synthetically manufacturedversion of a biologically available structure. Solid state layers can beformed from both organic and inorganic materials including, but notlimited to, microelectronic materials, insulating materials such asSi₃N₄, Al₂O₃, and SiO, organic and inorganic polymers such as polyamide,plastics such as Teflon® or elastomers such as two-componentaddition-cure silicone rubber, and glasses. The solid state layer may beformed from monatomic layers, such as graphene, or layers that are onlya few atoms thick. Suitable graphene layers are disclosed inInternational Application No. PCT/US2008/010637 (published as WO2009/035647).

The method is typically carried out using (i) an artificial amphiphiliclayer comprising a pore, (ii) an isolated, naturally-occurring lipidbilayer comprising a pore, or (iii) a cell having a pore insertedtherein. The method is typically carried out using an artificialamphiphilic layer, such as an artificial lipid bilayer. The layer maycomprise other transmembrane and/or intramembrane proteins as well asother molecules in addition to the pore. Suitable apparatus andconditions are discussed below. The method of the invention is typicallycarried out in vitro.

The polynucleotide may be coupled to the membrane. This may be doneusing any known method. If the membrane is an amphiphilic layer, such asa lipid bilayer (as discussed in detail above), the polynucleotide ispreferably coupled to the membrane via a polypeptide present in themembrane or a hydrophobic anchor present in the membrane. Thehydrophobic anchor is preferably a lipid, fatty acid, sterol, carbonnanotube or amino acid.

The polynucleotide may be coupled directly to the membrane. Thepolynucleotide is preferably coupled to the membrane via a linker.Preferred linkers include, but are not limited to, polymers, such aspolynucleotides, polyethylene glycols (PEGs) and polypeptides. If apolynucleotide is coupled directly to the membrane, then some data willbe lost as the characterising run cannot continue to the end of thepolynucleotide due to the distance between the membrane and thehelicase. If a linker is used, then the polynucleotide can be processedto completion. If a linker is used, the linker may be attached to thepolynucleotide at any position. The linker is typically attached to thepolynucleotide at the tail polymer.

The coupling may be stable or transient. For certain applications, thetransient nature of the coupling is preferred. If a stable couplingmolecule were attached directly to either the 5′ or 3′ end of apolynucleotide, then some data will be lost as the characterising runcannot continue to the end of the polynucleotide due to the distancebetween the bilayer and the helicase's active site. If the coupling istransient, then when the coupled end randomly becomes free of thebilayer, then the polynucleotide can be processed to completion.Chemical groups that form stable or transient links with the membraneare discussed in more detail below. The polynucleotide may betransiently coupled to an amphiphilic layer, such as a lipid bilayerusing cholesterol or a fatty acyl chain. Any fatty acyl chain having alength of from 6 to 30 carbon atoms, such as hexadecanoic acid, may beused.

In preferred embodiments, the polynucleotide is coupled to anamphiphilic layer. Coupling of polynucleotides to synthetic lipidbilayers has been carried out previously with various differenttethering strategies. These are summarised in Table 7 below.

TABLE 7 Attachment group Type of coupling Reference Thiol StableYoshina-Ishii, C. and S. G. Boxer (2003). “Arrays of mobile tetheredvesicles on supported lipid bilayers.” J Am Chem Soc 125(13): 3696-7.Biotin Stable Nikolov, V., R. Lipowsky, et al. (2007). “Behavior ofgiant vesicles with anchored DNA molecules.” Biophys J 92(12): 4356-68Cholesterol Transient Pfeiffer, I. and F. Hook (2004). “Bivalentcholesterol- based coupling of oligonucletides to lipid membraneassemblies.” J Am Chem Soc 126(33): 10224-5 Lipid Stable van Lengerich,B., R. J. Rawle, et al. “Covalent attachment of lipid vesicles to afluid-supported bilayer allows observation of DNA-mediated vesicleinteractions.” Langmuir 26(11): 8666-72

Polynucleotides may be functionalized using a modified phosphoramiditein the synthesis reaction, which is easily compatible for the additionof reactive groups, such as thiol, cholesterol, lipid and biotin groups.These different attachment chemistries give a suite of attachmentoptions for polynucleotides. Each different modification group tethersthe polynucleotide in a slightly different way and coupling is notalways permanent so giving different dwell times for the polynucleotideto the bilayer. The advantages of transient coupling are discussedabove.

Coupling of polynucleotides can also be achieved by a number of othermeans provided that a reactive group can be added to the polynucleotide.The addition of reactive groups to either end of DNA has been reportedpreviously. A thiol group can be added to the 5′ of ssDNA usingpolynucleotide kinase and ATPγS (Grant, G. P. and P. Z. Qin (2007). “Afacile method for attaching nitroxide spin labels at the 5′ terminus ofnucleic acids.” Nucleic Acids Res 35(10): e77). A more diverse selectionof chemical groups, such as biotin, thiols and fluorophores, can beadded using terminal transferase to incorporate modifiedoligonucleotides to the 3′ of ssDNA (Kumar, A., P. Tchen, et al. (1988).“Nonradioactive labeling of synthetic oligonucleotide probes withterminal deoxynucleotidyl transferase.” Anal Biochem 169(2): 376-82).

Alternatively, the reactive group could be considered to be the additionof a short piece of DNA complementary to one already coupled to thebilayer, so that attachment can be achieved via hybridisation. Ligationof short pieces of ssDNA have been reported using T4 RNA ligase I(Troutt, A. B., M. G. McHeyzer-Williams, et al. (1992).“Ligation-anchored PCR: a simple amplification technique withsingle-sided specificity.” Proc Natl Acad Sci USA 89(20): 9823-5).Alternatively either ssDNA or dsDNA could be ligated to native dsDNA andthen the two strands separated by thermal or chemical denaturation. Tonative dsDNA, it is possible to add either a piece of ssDNA to one orboth of the ends of the duplex, or dsDNA to one or both ends. Then, whenthe duplex is melted, each single strand will have either a 5′ or 3′modification if ssDNA was used for ligation or a modification at the 5′end, the 3′ end or both if dsDNA was used for ligation. If thepolynucleotide is a synthetic strand, the coupling chemistry can beincorporated during the chemical synthesis of the polynucleotide. Forinstance, the polynucleotide can be synthesized using a primer with areactive group attached to it.

A common technique for the amplification of sections of genomic DNA isusing polymerase chain reaction (PCR). Here, using two syntheticoligonucleotide primers, a number of copies of the same section of DNAcan be generated, where for each copy the 5′ of each strand in theduplex will be a synthetic polynucleotide. By using an antisense primerthat has a reactive group, such as a cholesterol, thiol, biotin orlipid, each copy of the amplified target DNA will contain a reactivegroup for coupling.

The transmembrane pore is preferably a transmembrane protein pore. Atransmembrane protein pore is a polypeptide or a collection ofpolypeptides that permits hydrated ions, such as analyte, to flow fromone side of a membrane to the other side of the membrane. In the presentinvention, the transmembrane protein pore is capable of forming a porethat permits hydrated ions driven by an applied potential to flow fromone side of the membrane to the other. The transmembrane protein porepreferably permits analyte such as nucleotides to flow from one side ofthe membrane, such as a lipid bilayer, to the other. The transmembraneprotein pore allows a polynucleotide, such as DNA or RNA, to be movedthrough the pore.

The transmembrane protein pore may be a monomer or an oligomer. The poreis preferably made up of several repeating subunits, such as 6, 7, 8 or9 subunits. The pore is preferably a hexameric, heptameric, octameric ornonameric pore.

The transmembrane protein pore typically comprises a barrel or channelthrough which the ions may flow. The subunits of the pore typicallysurround a central axis and contribute strands to a transmembrane βbarrel or channel or a transmembrane α-helix bundle or channel.

The barrel or channel of the transmembrane protein pore typicallycomprises amino acids that facilitate interaction with analyte, such asnucleotides, polynucleotides or nucleic acids. These amino acids arepreferably located near a constriction of the barrel or channel. Thetransmembrane protein pore typically comprises one or more positivelycharged amino acids, such as arginine, lysine or histidine, or aromaticamino acids, such as tyrosine or tryptophan. These amino acids typicallyfacilitate the interaction between the pore and nucleotides,polynucleotides or nucleic acids.

Transmembrane protein pores for use in accordance with the invention canbe derived from β-barrel pores or α-helix bundle pores. β-barrel porescomprise a barrel or channel that is formed from β-strands. Suitableβ-barrel pores include, but are not limited to, β-toxins, such asα-hemolysin, anthrax toxin and leukocidins, and outer membraneproteins/porins of bacteria, such as Mycobacterium smegmatis porin(Msp), for example MspA, MspB, MspC or MspD, outer membrane porin F(OmpF), outer membrane porin G (OmpG), outer membrane phospholipase Aand Neisseria autotransporter lipoprotein (NalP). α-helix bundle porescomprise a barrel or channel that is formed from α-helices. Suitableα-helix bundle pores include, but are not limited to, inner membraneproteins and a outer membrane proteins, such as WZA and ClyA toxin. Thetransmembrane pore may be derived from Msp or from α-hemolysin (α-HL).

The transmembrane protein pore is preferably derived from Msp,preferably from MspA. Such a pore will be oligomeric and typicallycomprises 7, 8, 9 or 10 monomers derived from Msp. The pore may be ahomo-oligomeric pore derived from Msp comprising identical monomers.Alternatively, the pore may be a hetero-oligomeric pore derived from Mspcomprising at least one monomer that differs from the others. Preferablythe pore is derived from MspA or a homolog or paralog thereof.

A monomer derived from Msp typically comprises the sequence shown in SEQID NO: 2 or a variant thereof. SEQ ID NO: 2 is the MS-(B1)8 mutant ofthe MspA monomer. It includes the following mutations: D90N, D91N, D93N,D118R, D134R and E139K. A variant of SEQ ID NO: 2 is a polypeptide thathas an amino acid sequence which varies from that of SEQ ID NO: 2 andwhich retains its ability to form a pore. The ability of a variant toform a pore can be assayed using any method known in the art. Forinstance, the variant may be inserted into an amphiphilic layer alongwith other appropriate subunits and its ability to oligomerise to form apore may be determined. Methods are known in the art for insertingsubunits into membranes, such as amphiphilic layers. For example,subunits may be suspended in a purified form in a solution containing alipid bilayer such that it diffuses to the lipid bilayer and is insertedby binding to the lipid bilayer and assembling into a functional state.Alternatively, subunits may be directly inserted into the membrane usingthe “pick and place” method described in M. A. Holden, H. Bayley. J. Am.Chem. Soc. 2005, 127, 6502-6503 and International Application No.PCT/GB2006/001057 (published as WO 2006/100484).

Over the entire length of the amino acid sequence of SEQ ID NO: 2, avariant will preferably be at least 50% homologous to that sequencebased on amino acid identity. More preferably, the variant may be atleast 55%, at least 60%, at least 65%, at least 70%, at least 75%, atleast 80%, at least 85% at least 90% and more preferably at least 95%.97% or 99% homologous based on amino acid identity to the amino acidsequence of SEQ ID NO: 2 over the entire sequence. There may be at least80%, for example at least 85%, 90% or 95%, amino acid identity over astretch of 100 or more, for example 125, 150, 175 or 200 or more,contiguous amino acids (“hard homology”).

Standard methods in the art may be used to determine homology. Forexample the UWGCG Package provides the BESTFIT program which can be usedto calculate homology, for example used on its default settings(Devereux et al (1984) Nucleic Acids Research 12, p 387-395). The PILEUPand BLAST algorithms can be used to calculate homology or line upsequences (such as identifying equivalent residues or correspondingsequences (typically on their default settings)), for example asdescribed in Altschul S. F. (1993) J Mol Evol 36:290-300; Altschul, S. Fet al (1990) J Mol Biol 215:403-10. Software for performing BLASTanalyses is publicly available through the National Center forBiotechnology Information (http://www.ncbi.nlm.nih.gov/).

SEQ ID NO: 2 is the MS-(B1)8 mutant of the MspA monomer. The variant maycomprise any of the mutations in the MspB, C or D monomers compared withMspA. The mature forms of MspB, C and D are shown in SEQ ID NOs: 5 to 7.In particular, the variant may comprise the following substitutionpresent in MspB: A138P. The variant may comprise one or more of thefollowing substitutions present in MspC: A96G, N102E and A138P. Thevariant may comprise one or more of the following mutations present inMspD: Deletion of G1, L2V, E5Q, L8V, D13G, W21A, D22E, K47T, 149H, 168V,D91G, A96Q, N102D, S103T, V104I, S136K and G141A. The variant maycomprise combinations of one or more of the mutations and substitutionsfrom Msp B, C and D. The variant preferably comprises the mutation L88N.A variant of SEQ ID NO: 2 has the mutation L88N in addition to all themutations of MS-(B1)8 and is called MS-(B2)8. The pore used in theinvention is preferably MS-(B2)8. The further preferred variantcomprises the mutations G75S/G77S/L88N/Q126R. The variant of SEQ ID NO:2 has the mutations G75S/G77S/L88N/Q126R in addition to all themutations of MS-(B1)8 and is called MS-(B2C)8. The pore used in theinvention is preferably MS-(B2)8 or MS-(B2C)8.

Amino acid substitutions may be made to the amino acid sequence of SEQID NO: 2 in addition to those discussed above, for example up to 1, 2,3, 4, 5, 10, 20 or 30 substitutions. Conservative substitutions replaceamino acids with other amino acids of similar chemical structure,similar chemical properties or similar side-chain volume. The aminoacids introduced may have similar polarity, hydrophilicity,hydrophobicity, basicity, acidity, neutrality or charge to the aminoacids they replace. Alternatively, the conservative substitution mayintroduce another amino acid that is aromatic or aliphatic in the placeof a pre-existing aromatic or aliphatic amino acid. Conservative aminoacid changes are well-known in the art and may be selected in accordancewith the properties of the 20 main amino acids as defined in Table 8below. Where amino acids have similar polarity, this can also bedetermined by reference to the hydropathy scale for amino acid sidechains in Table 9.

TABLE 8 Chemical properties of amino acids Ala aliphatic, hydrophobic,neutral Met hydrophobic, neutral Cys polar, hydrophobic, neutral Asnpolar, hydrophilic, neutral Asp polar, hydrophilic, charged (−) Prohydrophobic, neutral Glu polar, hydrophilic, charged (−) Gln polar,hydrophilic, neutral Phe aromatic, hydrophobic, neutral Arg polar,hydrophilic, charged (+) Gly aliphatic, neutral Ser polar, hydrophilic,neutral His aromatic, polar, hydrophilic, Thr polar, hydrophilic,neutral charged (+) Ile aliphatic, hydrophobic, neutral Val aliphatic,hydrophobic, neutral Lys polar, hydrophilic, charged (+) Trp aromatic,hydrophobic, neutral Leu aliphatic, hydrophobic, neutral Tyr aromatic,polar, hydrophobic

TABLE 9 Hydropathy scale Side Chain Hydropathy Ile 4.5 Val 4.2 Leu 3.8Phe 2.8 Cys 2.5 Met 1.9 Ala 1.8 Gly −0.4 Thr −0.7 Ser −0.8 Trp −0.9 Tyr−1.3 Pro −1.6 His −3.2 Glu −3.5 Gln −3.5 Asp −3.5 Asn −3.5 Lys −3.9 Arg−4.5

One or more amino acid residues of the amino acid sequence of SEQ ID NO:2 may additionally be deleted from the polypeptides described above. Upto 1, 2, 3, 4, 5, 10, 20 or 30 residues may be deleted, or more.

Variants may include fragments of SEQ ID NO: 2. Such fragments retainpore forming activity. Fragments may be at least 50, 100, 150 or 200amino acids in length. Such fragments may be used to produce the pores.A fragment preferably comprises the pore forming domain of SEQ ID NO: 2.Fragments must include one of residues 88, 90, 91, 105, 118 and 134 ofSEQ ID NO: 2. Typically, fragments include all of residues 88, 90, 91,105, 118 and 134 of SEQ ID NO: 2.

One or more amino acids may be alternatively or additionally added tothe polypeptides described above. An extension may be provided at theamino terminal or carboxy terminal of the amino acid sequence of SEQ IDNO: 2 or polypeptide variant or fragment thereof. The extension may bequite short, for example from 1 to 10 amino acids in length.Alternatively, the extension may be longer, for example up to 50 or 100amino acids. A carrier protein may be fused to an amino acid sequenceaccording to the invention. Other fusion proteins are discussed in moredetail below.

As discussed above, a variant is a polypeptide that has an amino acidsequence which varies from that of SEQ ID NO: 2 and which retains itsability to form a pore. A variant typically contains the regions of SEQID NO: 2 that are responsible for pore formation. The pore formingability of Msp, which contains a β-barrel, is provided by β-sheets ineach subunit. A variant of SEQ ID NO: 2 typically comprises the regionsin SEQ ID NO: 2 that form β-sheets. One or more modifications can bemade to the regions of SEQ ID NO: 2 that form β-sheets as long as theresulting variant retains its ability to form a pore. A variant of SEQID NO: 2 preferably includes one or more modifications, such assubstitutions, additions or deletions, within its α-helices and/or loopregions.

The monomers derived from Msp may be modified to assist theiridentification or purification, for example by the addition of histidineresidues (a hist tag), aspartic acid residues (an asp tag), astreptavidin tag or a flag tag, or by the addition of a signal sequenceto promote their secretion from a cell where the polypeptide does notnaturally contain such a sequence. An alternative to introducing agenetic tag is to chemically react a tag onto a native or engineeredposition on the pore. An example of this would be to react a gel-shiftreagent to a cysteine engineered on the outside of the pore. This hasbeen demonstrated as a method for separating hemolysin hetero-oligomers(Chem Biol. 1997 July; 4(7):497-505).

The monomer derived from Msp may be labelled with a revealing label. Therevealing label may be any suitable label which allows the pore to bedetected. Suitable labels are described above.

The monomer derived from Msp may also be produced using D-amino acids.For instance, the monomer derived from Msp may comprise a mixture ofL-amino acids and D-amino acids. This is conventional in the art forproducing such proteins or peptides.

The monomer derived from Msp contains one or more specific modificationsto facilitate nucleotide discrimination. The monomer derived from Mspmay also contain other non-specific modifications as long as they do notinterfere with pore formation. A number of non-specific side chainmodifications are known in the art and may be made to the side chains ofthe monomer derived from Msp. Such modifications include, for example,reductive alkylation of amino acids by reaction with an aldehydefollowed by reduction with NaBH₄, amidination with methylacetimidate oracylation with acetic anhydride.

The monomer derived from Msp can be produced using standard methodsknown in the art. The monomer derived from Msp may be made syntheticallyor by recombinant means. For example, the pore may be synthesized by invitro translation and transcription (IVTT). Suitable methods forproducing pores are discussed in International Application Nos.PCT/GB09/001690 (published as WO 2010/004273), PCT/GB09/001679(published as WO 2010/004265) or PCT/GB10/000133 (published as WO2010/086603). Methods for inserting pores into membranes are discussed.

The transmembrane protein pore is also preferably derived fromα-hemolysin (α-HL). The wild type α-HL pore is formed of seven identicalmonomers or subunits (i.e. it is heptameric). The sequence of onemonomer or subunit of α-hemolysin-NN is shown in SEQ ID NO: 4. Thetransmembrane protein pore preferably comprises seven monomers eachcomprising the sequence shown in SEQ ID NO: 4 or a variant thereof.Amino acids 1, 7 to 21, 31 to 34, 45 to 51, 63 to 66, 72, 92 to 97, 104to 111, 124 to 136, 149 to 153, 160 to 164, 173 to 206, 210 to 213, 217,218, 223 to 228, 236 to 242, 262 to 265, 272 to 274, 287 to 290 and 294of SEQ ID NO: 4 form loop regions. Residues 113 and 147 of SEQ ID NO: 4form part of a constriction of the barrel or channel of α-HL.

In such embodiments, a pore comprising seven proteins or monomers eachcomprising the sequence shown in SEQ ID NO: 4 or a variant thereof arepreferably used in the method of the invention. The seven proteins maybe the same (homo-heptamer) or different (hetero-heptamer).

A variant of SEQ ID NO: 4 is a protein that has an amino acid sequencewhich varies from that of SEQ ID NO: 4 and which retains its poreforming ability. The ability of a variant to form a pore can be assayedusing any method known in the art. For instance, the variant may beinserted into an amphiphilic layer, such as a lipid bilayer, along withother appropriate subunits and its ability to oligomerise to form a poremay be determined. Methods are known in the art for inserting subunitsinto amphiphilic layers, such as lipid bilayers. Suitable methods arediscussed above.

The variant may include modifications that facilitate covalentattachment to or interaction with the helicase or construct. The variantpreferably comprises one or more reactive cysteine residues thatfacilitate attachment to the helicase or construct. For instance, thevariant may include a cysteine at one or more of positions 8, 9, 17, 18,19, 44, 45, 50, 51, 237, 239 and 287 and/or on the amino or carboxyterminus of SEQ ID NO: 4. Preferred variants comprise a substitution ofthe residue at position 8, 9, 17, 237, 239 and 287 of SEQ ID NO: 4 withcysteine (A8C, T9C, N17C, K237C, S239C or E287C). The variant ispreferably any one of the variants described in InternationalApplication No. PCT/GB09/001690 (published as WO 2010/004273),PCT/GB09/001679 (published as WO 2010/004265) or PCT/GB10/000133(published as WO 2010/086603).

The variant may also include modifications that facilitate anyinteraction with nucleotides.

The variant may be a naturally occurring variant which is expressednaturally by an organism, for instance by a Staphylococcus bacterium.Alternatively, the variant may be expressed in vitro or recombinantly bya bacterium such as Escherichia coli. Variants also includenon-naturally occurring variants produced by recombinant technology.Over the entire length of the amino acid sequence of SEQ ID NO: 4, avariant will preferably be at least 50% homologous to that sequencebased on amino acid identity. More preferably, the variant polypeptidemay be at least 55%, at least 60%, at least 65%, at least 70%, at least75%, at least 80%, at least 85%, at least 90% and more preferably atleast 95%, 97% or 99% homologous based on amino acid identity to theamino acid sequence of SEQ ID NO: 4 over the entire sequence. There maybe at least 80%, for example at least 85%, 90% or 95%, amino acididentity over a stretch of 200 or more, for example 230, 250, 270 or 280or more, contiguous amino acids (“hard homology”). Homology can bedetermined as discussed above.

Amino acid substitutions may be made to the amino acid sequence of SEQID NO: 4 in addition to those discussed above, for example up to 1, 2,3, 4, 5, 10, 20 or 30 substitutions. Conservative substitutions may bemade as discussed above.

One or more amino acid residues of the amino acid sequence of SEQ ID NO:4 may additionally be deleted from the polypeptides described above. Upto 1, 2, 3, 4, 5, 10, 20 or 30 residues may be deleted, or more.

Variants may be fragments of SEQ ID NO: 4. Such fragments retainpore-forming activity. Fragments may be at least 50, 100, 200 or 250amino acids in length. A fragment preferably comprises the pore-formingdomain of SEQ ID NO: 4. Fragments typically include residues 119, 121,135. 113 and 139 of SEQ ID NO: 4.

One or more amino acids may be alternatively or additionally added tothe polypeptides described above. An extension may be provided at theamino terminus or carboxy terminus of the amino acid sequence of SEQ IDNO: 4 or a variant or fragment thereof. The extension may be quiteshort, for example from 1 to 10 amino acids in length. Alternatively,the extension may be longer, for example up to 50 or 100 amino acids. Acarrier protein may be fused to a pore or variant.

As discussed above, a variant of SEQ ID NO: 4 is a subunit that has anamino acid sequence which varies from that of SEQ ID NO: 4 and whichretains its ability to form a pore. A variant typically contains theregions of SEQ ID NO: 4 that are responsible for pore formation. Thepore forming ability of α-HL, which contains a β-barrel, is provided byβ-strands in each subunit. A variant of SEQ ID NO: 4 typically comprisesthe regions in SEQ ID NO: 4 that form β-strands. The amino acids of SEQID NO: 4 that form β-strands are discussed above. One or moremodifications can be made to the regions of SEQ ID NO: 4 that formβ-strands as long as the resulting variant retains its ability to form apore. Specific modifications that can be made to the β-strand regions ofSEQ ID NO: 4 are discussed above.

A variant of SEQ ID NO: 4 preferably includes one or more modifications,such as substitutions, additions or deletions, within its α-helicesand/or loop regions. Amino acids that form α-helices and loops arediscussed above.

The variant may be modified to assist its identification or purificationas discussed above.

Pores derived from α-HL can be made as discussed above with reference topores derived from Msp.

In some embodiments, the transmembrane protein pore is chemicallymodified. The pore can be chemically modified in any way and at anysite. The transmembrane protein pore is preferably chemically modifiedby attachment of a molecule to one or more cysteines (cysteine linkage),attachment of a molecule to one or more lysines, attachment of amolecule to one or more non-natural amino acids, enzyme modification ofan epitope or modification of a terminus. Suitable methods for carryingout such modifications are well-known in the art. The transmembraneprotein pore may be chemically modified by the attachment of anymolecule. For instance, the pore may be chemically modified byattachment of a dye or a fluorophore.

Any number of the monomers in the pore may be chemically modified. Oneor more, such as 2, 3, 4, 5, 6, 7, 8, 9 or 10, of the monomers ispreferably chemically modified as discussed above.

The reactivity of cysteine residues may be enhanced by modification ofthe adjacent residues. For instance, the basic groups of flankingarginine, histidine or lysine residues will change the pKa of thecysteines thiol group to that of the more reactive S group. Thereactivity of cysteine residues may be protected by thiol protectivegroups such as dTNB. These may be reacted with one or more cysteineresidues of the pore before a linker is attached.

The molecule (with which the pore is chemically modified) may beattached directly to the pore or attached via a linker as disclosed inInternational Application Nos. PCT/GB09/001690 (published as WO2010/004273), PCT/GB09/001679 (published as WO 2010/004265) orPCT/GB10/000133 (published as WO 2010/086603).

The helicase or construct may be covalently attached to the pore. Thehelicase or construct is preferably not covalently attached to the pore.The application of a voltage to the pore and helicase or constructtypically results in the formation of a sensor that is capable ofsequencing target polynucleotides. This is discussed in more detailbelow.

Any of the proteins described herein, i.e. the helicases, thetransmembrane protein pores or constructs, may be modified to assisttheir identification or purification, for example by the addition ofhistidine residues (a his tag), aspartic acid residues (an asp tag), astreptavidin tag, a flag tag, a SUMO tag, a GST tag or a MBP tag, or bythe addition of a signal sequence to promote their secretion from a cellwhere the polypeptide does not naturally contain such a sequence. Analternative to introducing a genetic tag is to chemically react a tagonto a native or engineered position on the helicase, pore or construct.An example of this would be to react a gel-shift reagent to a cysteineengineered on the outside of the pore. This has been demonstrated as amethod for separating hemolysin hetero-oligomers (Chem Biol. 1997 July;4(7):497-505).

The helicase, pore or construct may be labelled with a revealing label.The revealing label may be any suitable label which allows the pore tobe detected. Suitable labels include, but are not limited to,fluorescent molecules, radioisotopes, e.g. ¹²⁵I, ³⁵S, enzymes,antibodies, antigens, polynucleotides and ligands such as biotin.

Proteins may be made synthetically or by recombinant means. For example,the helicase, pore or construct may be synthesized by in vitrotranslation and transcription (IVTT). The amino acid sequence of thehelicase, pore or construct may be modified to include non-naturallyoccurring amino acids or to increase the stability of the protein. Whena protein is produced by synthetic means, such amino acids may beintroduced during production. The helicase, pore or construct may alsobe altered following either synthetic or recombinant production.

The helicase, pore or construct may also be produced using D-aminoacids. For instance, the pore or construct may comprise a mixture ofL-amino acids and D-amino acids. This is conventional in the art forproducing such proteins or peptides.

The helicase, pore or construct may also contain other non-specificmodifications as long as they do not interfere with pore formation orhelicase or construct function. A number of non-specific side chainmodifications are known in the art and may be made to the side chains ofthe protein(s). Such modifications include, for example, reductivealkylation of amino acids by reaction with an aldehyde followed byreduction with NaBH₄, amidination with methylacetimidate or acylationwith acetic anhydride.

The helicase, pore and construct can be produced using standard methodsknown in the art. Polynucleotide sequences encoding a helicase, pore orconstruct may be derived and replicated using standard methods in theart. Polynucleotide sequences encoding a helicase, pore or construct maybe expressed in a bacterial host cell using standard techniques in theart. The helicase, pore and/or construct may be produced in a cell by insitu expression of the polypeptide from a recombinant expression vector.The expression vector optionally carries an inducible promoter tocontrol the expression of the polypeptide. These methods are describedin Sambrook, J. and Russell, D. (2001). Molecular Cloning: A LaboratoryManual, 3rd Edition. Cold Spring Harbor Laboratory Press, Cold SpringHarbor, N.Y.

The helicase, pore and/or construct may be produced in large scalefollowing purification by any protein liquid chromatography system fromprotein producing organisms or after recombinant expression. Typicalprotein liquid chromatography systems include FPLC, AKTA systems, theBio-Cad system, the Bio-Rad BioLogic system and the Gilson HPLC system.

The method of the invention involves measuring one or morecharacteristics of the target polynucleotide. The method may involvemeasuring two, three, four or five or more characteristics of the targetpolynucleotide. The one or more characteristics are preferably selectedfrom (i) the length of the target polynucleotide, (ii) the identity ofthe target polynucleotide, (iii) the sequence of the targetpolynucleotide, (iv) the secondary structure of the targetpolynucleotide and (v) whether or not the target polynucleotide ismodified. Any combination of (i) to (v) may be measured in accordancewith the invention.

For (i), the length of the polynucleotide may be measured for example bydetermining the number of interactions between the target polynucleotideand the pore or the duration of interaction between the targetpolynucleotide and the pore.

For (ii), the identity of the polynucleotide may be measured in a numberof ways. The identity of the polynucleotide may be measured inconjunction with measurement of the sequence of the targetpolynucleotide or without measurement of the sequence of the targetpolynucleotide. The former is straightforward; the polynucleotide issequenced and thereby identified. The latter may be done in severalways. For instance, the presence of a particular motif in thepolynucleotide may be measured (without measuring the remaining sequenceof the polynucleotide). Alternatively, the measurement of a particularelectrical and/or optical signal in the method may identify the targetpolynucleotide as coming from a particular source.

For (iii), the sequence of the polynucleotide can be determined asdescribed previously. Suitable sequencing methods, particularly thoseusing electrical measurements, are described in Stoddart D et al., ProcNatl Acad Sci, 12; 106(19):7702-7, Lieberman K R et al, J Am Chem Soc.2010; 132(50):17961-72, and International Application WO 2000/28312.

For (iv), the secondary structure may be measured in a variety of ways.For instance, if the method involves an electrical measurement, thesecondary structure may be measured using a change in dwell time or achange in current flowing through the pore. This allows regions ofsingle-stranded and double-stranded polynucleotide to be distinguished.

For (v), the presence or absence of any modification may be measured.The method preferably comprises determining whether or not the targetpolynucleotide is modified by methylation, by oxidation, by damage, withone or more proteins or with one or more labels, tags or spacers.Specific modifications will result in specific interactions with thepore which can be measured using the methods described below. Forinstance, methylcytosine may be distinguished from cytosine on the basisof the current flowing through the pore during its interaction with eachnucleotide.

A variety of different types of measurements may be made. This includeswithout limitation: electrical measurements and optical measurements.Possible electrical measurements include: current measurements,impedance measurements, tunneling measurements (Ivanov A P et al., NanoLett. 2011 Jan. 12; 11(1):279-85), and FET measurements (InternationalApplication WO 2005/124888). Optical measurements may be combined withelectrical measurements (Soni G V et al., Rev Sci Instrum. 2010 January;81(1):014301). The measurement may be a transmembrane currentmeasurement such as measurement of ionic current flowing through thepore.

Electrical measurements may be made using standard single channelrecording equipment as describe in Stoddart D et al., Proc Natl AcadSci, 12; 106(19):7702-7, Lieberman K R et al, J Am Chem Soc. 2010;132(50):17961-72, and International Application WO-2000/28312.Alternatively, electrical measurements may be made using a multi-channelsystem, for example as described in International ApplicationWO-2009/077734 and International Application WO-2011/067559.

In a preferred embodiment, the method comprises:

(a) contacting the target polynucleotide with a transmembrane pore and ahelicase of the invention or a construct of the invention such that thetarget polynucleotide moves through the pore and the helicase orconstruct controls the movement of the target polynucleotide through thepore; and

(b) measuring the current passing through the pore as the polynucleotidemoves with respect to the pore wherein the current is indicative of oneor more characteristics of the target polynucleotide and therebycharacterising the target polynucleotide.

The methods may be carried out using any apparatus that is suitable forinvestigating a membrane/pore system in which a pore is present in amembrane. The method may be carried out using any apparatus that issuitable for transmembrane pore sensing. For example, the apparatuscomprises a chamber comprising an aqueous solution and a barrier thatseparates the chamber into two sections. The barrier typically has anaperture in which the membrane containing the pore is formed.Alternatively the barrier forms the membrane in which the pore ispresent.

The methods may be carried out using the apparatus described inInternational Application No. PCT/GB08/000562 (WO 2008/102120).

The methods may involve measuring the current passing through the poreas the polynucleotide moves with respect to the pore. Therefore theapparatus may also comprise an electrical circuit capable of applying apotential and measuring an electrical signal across the membrane andpore. The methods may be carried out using a patch clamp or a voltageclamp. The methods preferably involve the use of a voltage clamp.

The methods of the invention may involve the measuring of a currentpassing through the pore as the polynucleotide moves with respect to thepore. Suitable conditions for measuring ionic currents throughtransmembrane protein pores are known in the art and disclosed in theExample. The method is typically carried out with a voltage appliedacross the membrane and pore. The voltage used is typically from +2 V to−2 V, typically −400 mV to +400 mV. The voltage used is preferably in arange having a lower limit selected from −400 mV, −300 mV, −200 mV, −150mV, −100 mV, −50 mV, −20 mV and 0 mV and an upper limit independentlyselected from +10 mV, +20 mV, +50 mV, +100 mV, +150 mV, +200 mV, +300 mVand +400 mV. The voltage used is more preferably in the range 100 mV to240 mV and most preferably in the range of 120 mV to 220 mV. It ispossible to increase discrimination between different nucleotides by apore by using an increased applied potential.

The methods are typically carried out in the presence of any chargecarriers, such as metal salts, for example alkali metal salt, halidesalts, for example chloride salts, such as alkali metal chloride salt.Charge carriers may include ionic liquids or organic salts, for exampletetramethyl ammonium chloride, trimethylphenyl ammonium chloride,phenyltrimethyl ammonium chloride, or 1-ethyl-3-methyl imidazoliumchloride. In the exemplary apparatus discussed above, the salt ispresent in the aqueous solution in the chamber. Potassium chloride(KCl), sodium chloride (NaCl), caesium chloride (CsCl) or a mixture ofpotassium ferrocyanide and potassium ferricyanide is typically used.KCl, NaCl and a mixture of potassium ferrocyanide and potassiumferricyanide are preferred. The salt concentration may be at saturation.The salt concentration may be 3 M or lower and is typically from 0.1 to2.5 M, from 0.3 to 1.9 M, from 0.5 to 1.8 M, from 0.7 to 1.7 M, from 0.9to 1.6 M or from 1 M to 1.4 M. The salt concentration is preferably from150 mM to 1 M. Hel308, XPD, RecD and TraI helicases surprisingly workunder high salt concentrations. The method is preferably carried outusing a salt concentration of at least 0.3 M, such as at least 0.4 M, atleast 0.5 M, at least 0.6 M, at least 0.8 M, at least 1.0 M, at least1.5 M, at least 2.0 M, at least 2.5 M or at least 3.0 M. High saltconcentrations provide a high signal to noise ratio and allow forcurrents indicative of the presence of a nucleotide to be identifiedagainst the background of normal current fluctuations.

The methods are typically carried out in the presence of a buffer. Inthe exemplary apparatus discussed above, the buffer is present in theaqueous solution in the chamber. Any buffer may be used in the method ofthe invention. Typically, the buffer is HEPES. Another suitable bufferis Tris-HCl buffer. The methods are typically carried out at a pH offrom 4.0 to 12.0, from 4.5 to 10.0, from 5.0 to 9.0, from 5.5 to 8.8,from 6.0 to 8.7 or from 7.0 to 8.8 or 7.5 to 8.5. The pH used ispreferably about 7.5.

The methods may be carried out at from 0° C. to 100° C., from 15° C. to95° C., from 16° C. to 90° C. from 17° C. to 85° C. from 18° C. to 80°C., 19° C. to 70° C., or from 20° C. to 60° C. The methods are typicallycarried out at room temperature. The methods are optionally carried outat a temperature that supports enzyme function, such as about 37° C.

The method may be carried out in the presence of free nucleotides orfree nucleotide analogues and/or an enzyme cofactor that facilitates theaction of the helicase or construct. The method may also be carried outin the absence of free nucleotides or free nucleotide analogues and inthe absence of an enzyme cofactor. The free nucleotides may be one ormore of any of the individual nucleotides discussed above. The freenucleotides include, but are not limited to, adenosine monophosphate(AMP), adenosine diphosphate (ADP), adenosine triphosphate (ATP),guanosine monophosphate (GMP), guanosine diphosphate (GDP), guanosinetriphosphate (GTP), thymidine monophosphate (TMP), thymidine diphosphate(TDP), thymidine triphosphate (TTP), uridine monophosphate (UMP),uridine diphosphate (UDP), uridine triphosphate (UTP), cytidinemonophosphate (CMP), cytidine diphosphate (CDP), cytidine triphosphate(CTP), cyclic adenosine monophosphate (cAMP), cyclic guanosinemonophosphate (cGMP), deoxyadenosine monophosphate (dAMP),deoxyadenosine diphosphate (dADP), deoxyadenosine triphosphate (dATP),deoxyguanosine monophosphate (dGMP), deoxyguanosine diphosphate (dGDP),deoxyguanosine triphosphate (dGTP), deoxythymidine monophosphate (dTMP),deoxythymidine diphosphate (dTDP), deoxythymidine triphosphate (dTTP),deoxyuridine monophosphate (dUMP), deoxyuridine diphosphate (dUDP),deoxyuridine triphosphate (dUTP), deoxycytidine monophosphate (dCMP),deoxycytidine diphosphate (dCDP) and deoxycytidine triphosphate (dCTP).The free nucleotides are preferably selected from AMP, TMP, GMP, CMP,UMP, dAMP, dTMP, dGMP or dCMP. The free nucleotides are preferablyadenosine triphosphate (ATP). The enzyme cofactor is a factor thatallows the helicase or construct to function. The enzyme cofactor ispreferably a divalent metal cation. The divalent metal cation ispreferably Mg²⁺, Mn²⁺, Ca²⁺ or Co²⁺. The enzyme cofactor is mostpreferably Mg²⁺.

The target polynucleotide may be contacted with the helicase orconstruct and the pore in any order. In is preferred that, when thetarget polynucleotide is contacted with the helicase or construct andthe pore, the target polynucleotide firstly forms a complex with thehelicase or construct. When the voltage is applied across the pore, thetarget polynucleotide/helicase or construct complex then forms a complexwith the pore and controls the movement of the polynucleotide throughthe pore.

As discussed above, helicases may work in two modes with respect to thepore. The helicases of the invention or the constructs of the inventioncan also work in two modes. First, the method is preferably carried outusing the helicase or construct such that it moves the target sequencethrough the pore with the field resulting from the applied voltage. Inthis mode the 3′ end of the DNA is first captured in the pore (for a3′-5′ helicase), and the helicase or construct moves the DNA into thepore such that the target sequence is passed through the pore with thefield until it finally translocates through to the trans side of thebilayer (See FIG. 8). Alternatively, the method is preferably carriedout such that the helicase or construct moves the target sequencethrough the pore against the field resulting from the applied voltage.In this mode the 5′ end of the DNA is first captured in the pore (for a3′-5′ helicase), and the helicase or construct moves the DNA through thepore such that the target sequence is pulled out of the pore against theapplied field until finally ejected back to the cis side of the bilayer(see FIG. 7).

Other Methods

The invention also provides a method of forming a sensor forcharacterising a target polynucleotide. The method comprises forming acomplex between a pore and a helicase of the invention or a construct ofthe invention. The complex may be formed by contacting the pore and thehelicase or construct in the presence of the target polynucleotide andthen applying a potential across the pore. The applied potential may bea chemical potential or a voltage potential as described above.Alternatively, the complex may be formed by covalently attaching thepore to the helicase or construct. Methods for covalent attachment areknown in the art and disclosed, for example, in InternationalApplication Nos. PCT/GB09/001679 (published as WO 2010/004265) andPCT/GB10/000133 (published as WO 2010/086603). The complex is a sensorfor characterising the target polynucleotide. The method preferablycomprises forming a complex between a pore derived from Msp and ahelicase of the invention or a construct of the invention. Any of theembodiments discussed above with reference to the methods of theinvention equally apply to this method. The invention also provides asensor produced using the method of the invention.

Kits

The present invention also provides a kit for characterising a targetpolynucleotide. The kit comprises (a) a pore and (b) a helicase of theinvention or a construct of the invention. Any of the embodimentsdiscussed above with reference to the method of the invention equallyapply to the kits.

The kit may further comprise the components of a membrane, such as thephospholipids needed to form an amphiphilic layer, such as a lipidbilayer.

The kit of the invention may additionally comprise one or more otherreagents or instruments which enable any of the embodiments mentionedabove to be carried out. Such reagents or instruments include one ormore of the following: suitable buffer(s) (aqueous solutions), means toobtain a sample from a subject (such as a vessel or an instrumentcomprising a needle), means to amplify and/or express polynucleotides, amembrane as defined above or voltage or patch clamp apparatus. Reagentsmay be present in the kit in a dry state such that a fluid sampleresuspends the reagents. The kit may also, optionally, compriseinstructions to enable the kit to be used in the method of the inventionor details regarding which patients the method may be used for. The kitmay, optionally, comprise nucleotides.

Apparatus

The invention also provides an apparatus for characterising a targetpolynucleotide. The apparatus comprises a plurality of pores and aplurality of helicases of the invention or a plurality of constructs ofthe invention. The apparatus preferably further comprises instructionsfor carrying out the method of the invention. The apparatus may be anyconventional apparatus for polynucleotide analysis, such as an array ora chip. Any of the embodiments discussed above with reference to themethods of the invention are equally applicable to the apparatus of theinvention.

The apparatus is preferably set up to carry out the method of theinvention.

The apparatus preferably comprises:

a sensor device that is capable of supporting the plurality of pores andbeing operable to perform polynucleotide characterisation using thepores and constructs; and at least one reservoir for holding materialfor performing the characterisation.

The apparatus preferably comprises:

a sensor device that is capable of supporting the plurality of pores andbeing operable to perform polynucleotide characterisation using thepores and helicases or constructs; and

at least one reservoir for holding material for performing thecharacterisation.

The apparatus preferably comprises:

a sensor device that is capable of supporting the membrane and pluralityof pores and being operable to perform polynucleotide characterisingusing the pores and helicases or constructs;

at least one reservoir for holding material for performing thecharacterising;

a fluidics system configured to controllably supply material from the atleast one reservoir to the sensor device; and one or more containers forreceiving respective samples, the fluidics system being configured tosupply the samples selectively from one or more containers to the sensordevice. The apparatus may be any of those described in InternationalApplication No. PCT/GB08/004127 (published as WO 2009/077734),PCT/GB10/000789 (published as WO 2010/122293), International ApplicationNo. PCT/GB10/002206 (not yet published) or International Application No.PCT/US99/25679 (published as WO 00/28312).

Methods of Producing Helicases of the Invention

The invention also provides methods of producing a helicase of theinvention. In one embodiment, the method comprises providing a helicaseformed from one or more monomers and comprising a polynucleotide bindingdomain which comprises an opening through which a polynucleotide canunbind from the helicase. Any of the helicases discussed above can beused in the methods.

The method also comprises modifying the helicase such that two or moreparts on the same monomer of the helicase are connected to reduce thesize of the opening. The site of and method of connection are selectedas discussed above.

In another embodiment, the method comprises providing a Hel308 helicase.Any of the Hel308 helicases described above may be used.

The method further comprises introducing one or more cysteine residuesand/or one or more non-natural amino acids at one or more of thepositions which correspond to D272, N273, D274, G281, E284, E285, E287,5288, T289, G290, E291, D293, T294, N300, R303, K304, N314, S315, N316,H317, R318, K319, L320, E322, R326, N328 and S615 in Hel308 Mbu (SEQ IDNO: 10).

The method preferably further comprises (c) heating the modifiedhelicase, for instance by heating at 50° C. for 10 minutes, (d) exposingthe modified helicase to UV light, for instance by exposing the modifiedhelicase to high intensity UV light at 254 nm for about 10 to about 15minutes or (e) exposing the modified helicase to ferrocyanide andferricyanide, such as potassium ferrocyanide and potassium ferricyanide.Any combination of steps (c), (d) and (e) may be performed, such as (c),(d), (e), (c) and (d), (d) and (e), (c) and (e) or (c), (d) and (e).

The method preferably further comprises determining whether or not thehelicase is capable of controlling the movement of a polynucleotide.Assays for doing this are described above. If the movement of apolynucleotide can be controlled, the helicase has been modifiedcorrectly and a helicase of the invention has been produced. If themovement of a polynucleotide cannot be controlled, a helicase of theinvention has not been produced.

Methods of Producing Constructs of the Invention

The invention also provides a method of producing a construct of theinvention. The method comprises attaching, preferably covalentlyattaching a helicase of the invention to an additional polynucleotidebinding moiety. Any of the helicases and moieties discussed above can beused in the methods. The site of and method of covalent attachment areselected as discussed above.

The method preferably further comprises determining whether or not theconstruct is capable of controlling the movement of a polynucleotide.Assays for doing this are described above. If the movement of apolynucleotide can be controlled, the helicase and moiety have beenattached correctly and a construct of the invention has been produced.If the movement of a polynucleotide cannot be controlled, a construct ofthe invention has not been produced.

The following Example illustrates the invention.

Example 1

This Example describes the method of synthesising the Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with the mutationsE284C/S615C connected by a bismaleimidePEG3 linker). In this case acovalent link between cysteines at positions 284 and 615 in the primarysequence of Hel308 Mbu (SEQ ID NO: 10) was made by reacting thesepositions with a bismaleimidePEG3 linker (approximately 3.7 nm inlength).

In detail, 6 μl of 1 M DTT was added to 600 μL of Hel308Mbu(E284C/S615C) (SEQ ID NO: 10 with the mutations E284C/S615C, storedin 50 mM Tris-HCl pH 8.0, 421 mM NaCl, 10% Glycerol, 10 mM DTT) and themixture was incubated at room temperature on a 10″ wheel rotating at 20rpm for 30 minutes. This mixture was buffer exchanged through Pierce 2mL Zeba desalting columns, 7k MWCO into 100 mM potassium phosphate, 500mM NaCl, 5 mM EDTA, 0.1% Tween-20 pH 8.0 to give 550 μL of sample. Tothis was added, 5.5 μL of bismaleimidePEG3 (QuantaBiodesign, ProductRef=10215) and the mixture incubated at room temperature on a 10″ wheelrotating at 20 rpm for 120 minutes. To stop the reaction, 5.5 μL of 1 MDTT was added to quench any remaining maleimides. Analysis of thereaction was by 7.5% polyacrylamide gel or by reverse phase HPLC(chromatographed on a Jupiter C5 300A 5 μm 150×4.6 mm column, using agradient of acetonitrile in 0.1% TFA). FIG. 1 shows a coomassie stained7.5% Tris-HCl gel (loaded with Laemmli loading buffer) of the Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with the mutationsE284C/S615C connected by a bismaleimidePEG3 linker) reaction mixture.Lane X shows an appropriate protein ladder (the mass unit markers areshown on the left of the gel). Lanes a-c contain 2 μL, 5 μL or 10 μL ofapproximately 2.5 μM Hel308 Mbu(E284C/S615C) monomer (SEQ ID NO: 10 withmutations E284C/S615C). Lanes d-f contain 2 μL, 5 μL or 10 μL ofapproximately 2.5 μM Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ IDNO: 10 with the mutations E284C/S615C connected by a bismaleimidePEG3linker), it was clear from the gel that the reaction to attach thebismaleimidePEG3 linker went to nearly 100% yield. The Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with the mutationsE284C/S615C connected by a bismaleimidePEG3 linker) was then bufferexchanged to 50 mM Tris, 500 mM NaCl, 2 mM DTT, 10% glycerol pH 8.0.

Example 2

This example describes the method of synthesising the Hel308 Mbu(E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutations E284C/S615Cconnected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide, SEQ IDNO: 109 corresponds to the peptide sequence SRDFWRS)). In this case acovalent link between cysteines at positions 284 and 615 in the primarysequence of Hel308 Mbu (SEQ ID NO: 10) was made by reacting thesepositions with a bismaleimide peptide linker(maleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide, SEQ IDNO: 109 corresponds to the peptide sequence SRDFWRS).

In detail, 2 μl of 1 M DTT was added to 200 μL of Hel308Mbu(E284C/S615C) (SEQ ID NO: 10 with the mutations E284C/S615C, storedin 50 mM Tris-HCl pH 8.0, 421 mM NaCl, 10% Glycerol, 10 mM DTT) and themixture was incubated at room temperature on a 10″ wheel rotating at 20rpm for 30 minutes. This mixture was buffer exchanged through Pierce 2mL Zeba desalting columns, 7k MWCO into 100 mM potassium phosphate, 500mM NaCl, 5 mM EDTA, 0.1% Tween-20 pH 8.0 to give 540 μL of sample. To analiquot of 100 ul, 0.5 ul of 10 mMmaleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide (PPRL,Product Ref=16450) was added and the mixture incubated at roomtemperature on a 10″ wheel rotating at 20 rpm for 120 minutes. To stopthe reaction, 1 ul of 1 M DTT was added to quench any remainingmaleimides. Analysis of the reaction is by 7.5% polyacrylamide gel or byreverse phase HPLC (chromatographed on a Jupiter C5 300A 5 μm 150×4.6 mmcolumn, using a gradient of acetonitrile in 0.1% TFA). FIG. 2 shows acoomassie stained 7.5% Tris-HCl gel of the Hel308 Mbu(E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutations E284C/S615Cconnected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide) reactionmixture. Lane X shows an appropriate protein ladder (the mass unitmarkers are shown on the left of the gel). Lane A contains 5 μL ofapproximately 10 μM Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO:10 with the mutations E284C/S615C connected by a bismaleimidePEG3linker) as a reference. The upper band corresponds to Hel308Mbu(E284C/S615C)-bismaleimidePEG3 and the lower band to Hel308 Mbu(E284C/S615C) (SEQ ID NO: 10 with the mutations E284C/S615C). Lane Bcontains 5 μL of approximately 10 μM Hel308 Mbu(E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutations E284C/S615Cconnected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide), it wasclear from the gel that the reaction to attach the mal-pep-mal linkerdid not go to completion as a band for the Hel308 Mbu(E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutations E284C/S615Cconnected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide) (upperband) and the Hel308 Mbu (E284C/S615C) (SEQ ID NO: 10 with the mutationsE284C/S615C) (lower band) are observed. Lane C contains Hel308 Mbu(E284C/S615C) (SEQ ID NO: 10 with the mutations E284C/S615C).

The Hel308 Mbu (E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with themutations E284C/S615C connected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS-(1,2-diaminoethane)-propyl-maleimide, SEQ IDNO: 109 corresponds to the peptide sequence SRDFWRS)) was then bufferexchanged to 50 mM Tris, 500 mM NaCl, 2 mM DTT, 10% glycerol pH 8.0.

Example 3

This example compares the enzyme processivity of two Hel308 Mbuhelicases in which the opening has been closed (Hel308Mbu(E284C/S615C)-bismaleimidePEG11 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG11) and Hel308Mbu(E284C/S615C)-bismaleimidePEG3) (SEQ ID NO: 10 with the mutationsE284C/S615C connected by a bismaleimidePEG3 linker) to that of theHel308 Mbu monomer (SEQ ID NO: 10) using a fluorescence based assay.

Materials and Methods

SEQ ID NOs: 110 to 114. SEQ ID NO: 112 has a carboxyfluorescein at the5′ end and a black-hole quencher at the 3′ end.

A custom fluorescent substrate was used to assay the ability of thehelicase to displace hybridised dsDNA (FIG. 3). The fluorescentsubstrate (50 nM final) has a 3′ ssDNA overhang, and 80 and 33 base-pairsections of hybridised dsDNA (FIG. 3 section A, SEQ ID NO: 110). Themajor lower “template” strand is hybridised to an 80 nt “blocker” strand(SEQ ID NO: 111), adjacent to its 3′ overhang, and a 33 nt fluorescentprobe, labelled at its 5′ and 3′ ends with carboxyfluorescein (FAM) andblack-hole quencher (BHQ-1) bases, respectively (SEQ ID NO: 112). Whenhybridised, the FAM is distant from the BHQ-1 and the substrate isessentially fluorescent. In the presence of ATP (1 mM) and MgCl₂ (10mM), the helicase (10 nM) binds to the substrate's 3′ overhang (SEQ IDNO: 110), moves along the lower strand, and begins to displace the 80 ntblocker strand (SEQ ID NO: 111), as shown in FIG. 3 section B. Ifprocessive, the helicase displaces the fluorescent probe (SEQ ID NO:112, labelled with a carboxyfluorescein (FAM) at its 5′ end a black-holequencher (BHQ-1) at its 3′ end) too (FIG. 3 section C). The fluorescentprobe is designed in such a way that its 5′ and 3′ ends areself-complementary and thus form a kinetically-stable hairpin oncedisplaced, preventing the probe from re-annealing to the template strand(FIG. 3 section D). Upon formation of the hairpin product, the FAM isbrought into the vicinity of the BHQ-1 and its fluorescence is quenched.A processive enzyme, capable of displacing the 80 mer “blocker” (SEQ IDNO: 111) and fluorescent (SEQ ID NO: 112, labelled with acarboxyfluorescein (FAM) at its 5′ end a black-hole quencher (BHQ-1) atits 3′ end) strands will therefore lead to a decrease in fluorescenceover time. However, if the enzyme has a processivity of less than 80 ntit would be unable to displace the fluorescent strand (SEQ ID NO: 112,labelled with a carboxyfluorescein (FAM) at its 5′ end a black-holequencher (BHQ-1) at its 3′ end) and, therefore, the “blocker” strand(SEQ ID NO: 111) would reanneal to the major bottom strand (FIG. 3section E, SEQ ID NO: 110).

Additional custom fluorescent substrates were also used for controlpurposes. The substrate used as a negative control was identical to thatof the one described in FIG. 3 but lacking the 3′ overhang (FIG. 4section A, (SEQ ID NOs: 111, 112 (labelled with a carboxyfluorescein(FAM) at its 5′ end a black-hole quencher (BHQ-1) at its 3′ end) and113)). A similar substrate to that described in FIG. 3 but lacking the80 base pair section, used as a positive control for active, but notnecessarily processive, helicases (FIG. 4 section B, (SEQ ID NO's: 112(labelled with a carboxyfluorescein (FAM) at its 5′ end a black-holequencher (BHQ-1) at its 3′ end) and 114)).

FIG. 5 shows a graph of the time-dependent fluorescence changes upontesting Hel308 Mbu monomer (SEQ ID NO: 10), Hel308Mbu(E284C/S615C)-bismaleimidePEG11 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG11 linker) and Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker) against theprocessivity substrate shown in FIG. 3 in buffered solution (400 mMNaCl, 10 mM Hepes pH 8.0, 1 mM ATP, 10 mM MgCl₂, 50 nM fluorescentsubstrate DNA (SEQ ID NOs: 110, 111 and 112 (labelled with acarboxyfluorescein (FAM) at its 5′ end a black-hole quencher (BHQ-1) atits 3′ end))). The decrease in fluorescence exhibited by Hel308Mbu(E284C/S615C)-bismaleimidePEG11 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG11 linker) and Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker), denote theincreased processivity of these complexes as compared to Hel308 Mbumonomer (SEQ ID NO: 10). FIG. 6 shows positive controls demonstratingthat all helicases were indeed active, as denoted by a fluorescencedecrease for all samples.

Example 4

This example compares the ability of a Hel308 Mbu monomer (SEQ ID NO:10), to control the movement of intact DNA strands (900 mer) through ananopore, to that of the Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQID NO. 10 with the following mutations E284C/S615C connected by abismaleimidePEG3 linker). The general method for controlled DNAtranslocation against the field is shown in FIG. 7 and with the field inFIG. 8.

Materials and Methods

The DNA was formed by ligating a 50-polyT 5′ leader to a 900 basefragment of PhiX dsDNA. The leader also contains a complementary sectionto which SEQ ID NO: 117 (which at the 3′ end of the sequence has sixiSp18 spacers attached to two thymine residues and a 3′ cholesterol TEG)was hybridized to allow the DNA to be tethered to the bilayer. Finallythe 3′ end of the PhiX dsDNA was digested with AatII digestion enzyme toyield a 4 nt 3-overhang of ACGT (see FIG. 9 for diagram of the DNAsubstrate design).

Buffered solution used for Hel308 Mbu: 400 mM NaCl, 100 mM Hepes, 10 mMpotassium ferrocyanide, 10 mM potassium ferricyanide pH8.0, 1 mM ATP, 1mM MgCl₂,Buffered solution used for Hel308 Mbu(E284C/S615C)-bismaleimidePEG3: 400mM NaCl, 100 mM Hepes, 10 mM potassium ferrocyanide, 10 mM potassiumferricyanide pH8.0, 2 mM ATP, 2 mM MgCl₂,Nanopore: E. coli MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 withthe mutations G75S/G77S/L88N/Q126R)Enzymes: Hel308 Mbu (SEQ ID NO: 10) added at 200 nM final and Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with the followingmutations E284C/S615C connected by a bismaleimide3PEG linker) added at10 nM final.

Electrical measurements were acquired from single MspA nanoporesinserted in 1,2-diphytanoyl-glycero-3-phosphocholine lipid (Avanti PolarLipids) bilayers. Bilayers were formed across ˜100 um diameter aperturesin 20 um thick PTFE films (in custom Delrin chambers) via theMontal-Mueller technique, separating two 1 mL buffered solutions. Allexperiments were carried out in the stated buffered solution.Single-channel currents were measured on Axopatch 200B amplifiers(Molecular Devices) equipped with 1440A digitizers. Platinum electrodesare connected to the buffered solutions so that the cis compartment (towhich both nanopore and enzyme/DNA are added) is connected to the groundof the Axopatch headstage, and the trans compartment is connected to theactive electrode of the headstage.

After achieving a single pore in the bilayer, DNA complex (SEQ ID NOs:115, 116 and 117 (which at the 3′ end of the sequence has six iSp18spacers attached to two thymine residues and a 3′ cholesterol TEG)),DNA=0.1 nM for the Hel308 Mbu monomer (SEQ ID NO: 10) and 0.05 nM forthe Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 withmutations E284C/S615C connected by a bismaleimidePEG3 linker), MgCl₂ (2mM) and ATP (2 mM) were added to the cis compartment of theelectrophysiology chamber. A control experiment was run at +140 mV. Thehelicase Hel308 Mbu monomer (SEQ ID NO: 10, 200 nM) or the Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker, 10 nM) was thenadded to the cis compartment. Experiments were carried out at a constantpotential of +140 mV.

Results and Discussion

The addition of helicase monomer-DNA substrate to MspA nanopores (asshown in FIG. 7) produces characteristic current blocks as shown in FIG.10. The helicase Hel308 Mbu monomer (SEQ ID NO: 10) is able to move DNAthrough a nanopore in a controlled fashion, producing stepwise changesin current as the DNA moves through the nanopore. Example current tracesobserved when a helicase controls the translocation of DNA (+140 mV, 400mM NaCl, 100 mM Hepes pH 8.0, 10 mM potassium ferrocyanide, 10 mMpotassium ferricyanide, 0.1 nM 900mer DNA (SEQ ID NOs: 115, 116 and 117(which at the 3′ end of the sequence has six iSp18 spacers attached totwo thymine residues and a 3′ cholesterol TEG)), 1 mM ATP, 1 mM MgCl₂)through an MspA nanopore (MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO:2 with mutations G75S/G77S/L88N/Q126R) using Hel308 Mbu (200 nM, SEQ IDNO: 10) are shown in FIG. 10. The top electrical trace shows the openpore current (˜120 pA) dropping to a DNA level (20-50 pA) when DNA iscaptured under the force of the applied potential (+140 mV). DNA with anenzyme attached results in a long block that shows stepwise changes incurrent as the enzyme moves the DNA through the pore. The upper traceshows a sequence of 8 separate helicase-controlled DNA movements markedA-H (see FIG. 10). All the helicase-controlled DNA movements in thissection of trace are being moved through the nanopore against the fieldby the enzyme (DNA captured 5′ down) (see FIG. 7 for details). Below areenlargements of the last section of 4 of the helicase-controlled DNAmovements as the DNA exits the nanopore. Of the 8 helicase-controlledDNA movements in this section, only 1 (H) ends in the characteristiclong polyT level that indicates that the enzyme has reached the end ofthe DNA and moved the 50T 5′-leader of the DNA substrate through thepore. In the full run with Hel308 Mbu monomer (SEQ ID NO: 10) it wasfound that ˜30% of the helicase-controlled DNA movements end at thepolyT (n=19 helicase-controlled DNA movements in this experiment).

The Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (10 nM, SEQ ID NO: 10 withmutations E284C/S615C connected by a bismaleimidePEG3 linker) is able tomove DNA through a nanopore in a controlled fashion against the field,producing stepwise changes in current as the DNA moves through thenanopore. Example current traces observed when a helicase controls thetranslocation of DNA (+140 mV, 400 mM NaCl, 100 mM Hepes pH 8.0, 10 mMpotassium ferrocyanide, 10 mM potassium ferricyanide, 0.05 nM 900mer DNA(SEQ ID NO: 115, 116 and 117 (which at the 3′ end of the sequence hassix iSp18 spacers attached to two thymine residues and a 3′ cholesterolTEG)), 2 mM ATP, 2 mM MgCl₂) through an MspA nanopore(MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 with mutationsG75S/G77S/L88N/Q126R) using the Hel308 Mbu(E284C/S615C)-bismaleimidePEG3(10 nM, SEQ ID NO: 10 with mutations E284C/S615C connected by abismaleimidePEG3 linker) are shown in FIG. 11. The top electrical traceshows the open pore current (˜115 pA) dropping to a DNA level (15-40 pA)when DNA is captured under the force of the applied potential (+140 mV).DNA with enzyme attached results in a long block that shows stepwisechanges in current as the enzyme moves the DNA through the pore. Theupper trace shows a sequence of 8 separate helicase-controlled DNAmovements marked A-H (see FIG. 11). All the helicase-controlled DNAmovements in this section of trace are being moved through the nanoporeagainst the field by the enzyme (DNA captured 5′ down) (see FIG. 7 fordetails). Below are enlargements of the last section of 4 of thehelicase-controlled DNA movements as the DNA exits the nanopore. Of the8 helicase-controlled DNA movements in this section, every one ends inthe characteristic long polyT level that indicates that the enzyme hasreached the end of the DNA and moved the 50T 5′-leader of the DNAsubstrate through the pore. In the full run with Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker) it was found that˜85% of the helicase-controlled DNA movements against the field (5′down) end at the polyT (n=27 helicase-controlled DNA movements in thisexperiment), thus demonstrating substantially improved processivityrelative to the unmodified Hel308 Mbu This experiment required only 10nM enzyme in order to observe helicase-controlled DNA movement, however,Hel308 Mbu monomer (SEQ ID NO: 10) experiments used 200 nM enzyme.Therefore, much lower enzyme concentrations of the helicases in whichthe opening has been closed can be used while still achieving long readlengths.

Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker) shows enhancedability to move DNA through a nanopore with the force of the appliedfield (see FIG. 8 for details), producing stepwise changes in current asthe DNA moves through the nanopore. Example current traces observed whena helicase controls the translocation of DNA (+140 mV, 400 mM NaCl, 100mM Hepes pH 8.0, 10 mM potassium ferrocyanide, 10 mM potassiumferricyanide, 0.05 nM 900mer DNA (SEQ ID NO: 115, 116 and 117 (which atthe 3′ end of the sequence has six iSp18 spacers attached to two thymineresidues and a 3′ cholesterol TEG)), 2 mM ATP, 2 mM MgCl₂) through anMspA nanopore (MS(B1-G75S/G77S/L88N/Q126R)8 MspA(SEQ ID NO: 2 withmutations G75S/G77S/L88N/Q126R) using the Hel308Mbu(E284C/S615C)-bismaleimidePEG3 (10 nM, SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker) are shown in FIG.12. The top electrical trace shows the open pore current (˜120 pA)dropping to a DNA level (15-40 pA) when DNA is captured under the forceof the applied potential (+140 mV). DNA with enzyme attached results ina long block that shows stepwise changes in current as the enzyme movesthe DNA through the pore. The upper trace shows a sequence of 4 separatehelicase-controlled DNA movements marked A-D (see FIG. 12). All thehelicase-controlled DNA movements in this section of trace are beingmoved through the nanopore with the field by the enzyme (DNA captured 3′down) (see FIG. 8 for details). Below are enlargements of the lastsection of the helicase-controlled DNA movements as the DNA exits thenanopore. 3′ down DNA shows a characteristically different signature to5′ down DNA, with a different current to sequence relationship, anddifferent variance. Of the 4 helicase-controlled DNA movements in thissection, every one ends in the characteristic long polyT level thatindicates that the enzyme has reached the end of the DNA and moved the50T 5′-leader of the DNA substrate through the pore. In the full runwith Hel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 withmutations E284C/S615C connected by a bismaleimidePEG3 linker) it wasfound that ˜87% of helicase-controlled DNA movements with the field (3′down) end at the polyT (n=15 helicase-controlled DNA movements in thisexperiment). In comparison, 3′ down helicase-controlled DNA movementsare rarely observed when using Hel308 Mbu monomer (SEQ ID NO: 10), andwhen they are the movements are short with typically less than 50 statesobserved, indicating a high level of enzyme dissociation in thisorientation. The long 3′ down helicase-controlled DNA movements, withHel308 Mbu(E284C/S615C)-bismaleimidePEG3 (SEQ ID NO: 10 with mutationsE284C/S615C connected by a bismaleimidePEG3 linker), show a surprisingimprovement in processivity in the 3′ down mode.

Example 5

This example shows that the Hel308 Mbu (E284C/S615C)-mal-pep-mal (SEQ IDNO: 10 with the mutations E284C/S615C connected by a bismaleimidepeptide linker (maleimide-propyl-SRDFWRS (SEQ ID NO:109)-(1,2-diaminoethane)-propyl-maleimide)) has the ability to controlthe movement of intact DNA strands (SEQ ID NO: 127 attached at its 3′end to four iSpC3 spacers, the last of which is attached to the 5′ endof SEQ ID NO: 128) through a nanopore. The general method for controlledDNA translocation against the field is shown in FIG. 7 and with thefield in FIG. 8.

Materials and Methods

Prior to setting up the experiment, the DNA (0.5 nM, (SEQ ID NO: 127attached at its 3′ end to four iSpC3 spacers, the last of which isattached to the 5′ end of SEQ ID NO: 128) and Hel308 Mbu(E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutations E284C/S615Cconnected by a bismaleimide peptide linker (maleimide-propyl-SRDFWRS(SEQ ID NO: 109)-(1,2-diaminoethane)-propyl-maleimide)) werepre-incubated together for 1 hour.

Electrical measurements were acquired from single MspA nanopores(MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 with mutationsG75S/G77S/L88N/Q126R) inserted in block co-polymer in buffer (625 mMKCl, 100 mM Hepes, 75 mM Potassium Ferrocyanide (II), 25 mM Potassiumferricyanide (III), pH 8). MgCl₂ (10 mM) and ATP (1 mM) were mixedtogether with buffer (625 mM KCl, 100 mM Hepes, 75 mM PotassiumFerrocyanide (II), 25 mM Potassium ferricyanide (III), pH 8) and thenadded to the DNA (SEQ ID NO: 127 attached at its 3′ end to four iSpC3spacers, the last of which is attached to the 5′ end of SEQ ID NO: 128),Hel308 Mbu (E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutationsE284C/S615C connected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS (SEQ ID NO:109)-(1,2-diaminoethane)-propyl-maleimide)) pre-mix. After achieving asingle pore in the bilayer, the pre-mix was added to the single nanoporeexperimental system. Experiments were carried out at a constantpotential of +120 mV and helicase-controlled DNA movement was monitored.

Results and Discussion

Helicase controlled DNA movement was observed for the closed complexHel308 Mbu (E284C/S615C)-mal-pep-mal (SEQ ID NO: 10 with the mutationsE284C/S615C connected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS (SEQ ID NO:109)-(1,2-diaminoethane)-propyl-maleimide)). An example of ahelicase-controlled DNA movement is shown in FIG. 13.

Example 6

This example describes the method of synthesising the TrwCCba-N691C/Q346C-PEG11 (SEQ ID NO: 126 with the mutations N691C/Q346Cconnected by a PEG11 linker). In this case a covalent link betweencysteines at positions 346 and 691 in the primary sequence of TrwC Cba(SEQ ID NO: 126) was made by reacting these positions with a PEG11linker.

Materials and Methods

In detail, DTT (2 μl, 1 M) was added to TrwC Cba-N691C/Q346C (200 μl,SEQ ID NO: 126 with the mutations N691C/Q346C, stored in 50 mM Hepes,10% glycerol, 10 mM DTT, 692 mM NaCl pH7.5) and the mixture wasincubated at room temperature on a 10″ wheel rotating at 20 rpm for 30minutes. This mixture was buffer exchanged through Pierce 2 mL Zebadesalting columns, 7 k MWCO into 100 mM potassium phosphate, 500 mMNaCl, 5 mM EDTA, 0.1% Tween-20 pH 8.0 and diluted in the same buffer togive 10 μL aliquots of sample. Maleimide-PEGI1-maleimide (50 uM finalconcentration, Quanta Biodesign, product #10397) was added to one of thealiquots and the mixture incubated at room temperature on a 10″ wheelrotating at 20 rpm for 120 minutes. To stop the reaction, DTT (1 ul of 1M) was added to quench any remaining maleimides. Analysis of thereaction is by 7.5% polyacrylamide gel. FIG. 14 shows a coomassiestained 7.5% Tris-HCl gel of the TrwC Cba-N691C/Q346C-mal-PEG11-mal (SEQID NO: 126 with the mutations N691C/Q346C connected by a bismaleimidepolyethylene glycol linker) reaction mixture. The lane on the right ofthe gel (labelled M) shows an appropriate protein ladder (the mass unitmarkers are shown on the right of the gel). Lane 1 contains 5 μL ofapproximately 10 μM TrwC Cba-D657C/R339C alone (SEQ ID NO: 126 withmutation D657C/R339C) as a reference. Lane 2 contains 5 μL ofapproximately 10 μM TrwC Cba-N691C/Q346C-bismaleimdiePEG11 (SEQ ID NO:126 with the mutations N691C/Q346C connected by a bismaleimide PEG11linker). As indicated in lane 2, the upper band corresponds to thedimeric enzyme species (labelled A), the middle band corresponds to theclosed complex (labelled B) TraI-Cba-N691C/Q346C-bismaleimidePEG1 (SEQID NO: 126 with the mutations N691C/Q346C connected by a bismaleimidePEG11 linker). It was clear from the gel that the reaction to attach themal-PEG11-mal linker did not go to completion as a band for unmodifiedstarting material (labelled C) TrwC Cba-N691C/Q346C (SEQ ID NO: 126 withthe mutations N691C/Q346C) was observed.

The TrwC Cba-N691C/Q346C-PEG11 (SEQ ID NO: 126 with the mutationsN691C/Q346C connected by a PEG11 linker) was then buffer exchanged to 50mM Tris, 500 mM NaCl, 2 mM DTT, pH 8.0.

Using an analogous procedure to that described in this example, it waspossible to make the following closed complexes listed in Table 10below.

TABLE 10 Entry No. Closed complex Sequence I TrwC Cba-N691C/Q346C- SEQID NO: 126 with the mutations N691C/Q346C mal-pep-mal connected by abismaleimide peptide linker (maleimide- propyl-SRDFWRS (SEQ lD NO:109)-(1,2- diaminoethane)-propyl-maleimide) 2 TrwC Cba-N691C/Q346C- SEQID NO: 126 with the mutations N691C/Q346C bismaleimidePEG3 connected bya bismaleimide PEG3 linker 3 TrwC Cba-D657C/R339C- SEQ ID NO: 126 withthe mutations D657C/R339C mal-pep-mal connected by a bismaleimidepeptide linker (maleimide- propyl-SRDFWRS (SEQ ID NO: 109)-(1,2-diaminoethane)-propyl-maleimide) 4 TrwC Cba-D657C/R339C- SEQ ID NO: 126with the mutations D657C/R339C bismaleimidePEG3 connected by abismaleimide PEG3 linker 5 TrwC Cba-D657C/R339C- SEQ ID NO: 126 with themutations D657C/R339C bismaleimidePEG11 connected by a bismaleimidePEG11 linker 6 TrwC Cba-N691C/S350C- SEQ ID NO: 126 with the mutationsN691C/S350C mal-pep-mal connected by a bismaleimide peptide linker(maleimide- propyl-SRDFWRS (SEQ ID NO: 109)-(1,2-diaminoethane)-propyl-maleimide) 7 TrwC Cba-N691C/S350C- SEQ ID NO:126with the mutations N691C/S350C bismaleimidePEG3 connected by abismaleimide PEG3 linker 8 TrwC Cba-N691C/S350C- SEQ ID NO:126 with themutations N691C/S350C bismaleimidePEG11 connected by a bismaleimidePEG11 linker 9 TrwC Cba-V690C/S350C- SEQ ID NO: 126 with the mutationsV690C/S350C mal-pep-mal connected by a bismaleimide peptide linker(maleimide-propyl-SRDFWRS (SEQ ID NO: 109)-(1,2-diaminoethane)-propyl-maleimide) 10 TrwC Cba-V690C/S350C- SEQ ID NO:126with the mutations V690C/S350C bismaleimidePEG3 connected by abismaleimide PEG3 linker 11 TrwC Cba-V690C/S350C- SEQ ID NO: 126 withthe mutations V690C/S350C bismaleimidePEG11 connected by a bismaleimidePEG11 linker

Example 7

This Example illustrates that when a number of helicases wereinvestigated (Hel308 Mbu (SEQ ID NO: 10), Hel308 Mbu-E284C (SEQ ID NO:10 with the mutation E284C), Hel308 Mbu-E284C/C301A (SEQ ID NO: 10 withthe mutations E284C/C301A), Hel308 Mbu-E285C (SEQ ID NO: 10 with themutation E285C), Hel308 Mbu-S288C (SEQ ID NO: 10 with the mutationS288C), and Hel308 Mbu-D274C (SEQ ID NO: 10 with the mutation D274C) fortheir rate of turnover of dsDNA molecules (min⁻¹enzyme⁻¹) using afluorescent assay, the mutant helicases (Hel308 Mbu-E284C (SEQ ID NO: 10with the mutation E284C), Hel308 Mbu-E284C/C301A (SEQ ID NO: 10 with themutations E284C/C301A), Hel308 Mbu-E285C (SEQ ID NO: 10 with themutation E285C), Hel308 Mbu-S288C (SEQ ID NO: 10 with the mutationS288C), and Hel3081Mbu-D274C (SEQ ID NO: 10 with the mutation D274C))tested had increased rate of turnover of dsDNA molecules (min⁻¹enzyme⁻¹)in comparison to Hel308 Mbu (SEQ ID NO: 10).

Materials and Methods

A custom fluorescent substrate was used to assay the ability of a numberof Hel308 Mbu helicases (Hel308 Mbu-E284C (SEQ ID NO: 10 with themutation E284C), Hel308 Mbu-E284C/C301A (SEQ ID NO: 10 with themutations E284C/C301A), Hel308 Mbu-E285C (SEQ ID NO: 10 with themutation E285C), Hel308 Mbu-S288C (SEQ ID NO: 10 with the mutationS288C), and Hel308 Mbu-D274C (SEQ ID NO: 10 with the mutation D274C)) todisplace hybridised dsDNA. As shown in 1) of FIG. 15, the fluorescentsubstrate strand (50 nM final) has both a 3′ and 5′ ssDNA overhang, anda 44 base section of hybridised dsDNA. The upper strand, containing the3′ ssDNA overhang, has a carboxyfluorescein base (the carboxyfluorescein(labelled c in FIG. 15) is attached to a thymine at position 6 in SEQ IDNO: 151) at the 5′ end, and the hybrised complement has a black-holequencher (BHQ-1, labelled e in FIG. 15) base (the black-hole quencher isattached to a thymine at position 81 in SEQ ID NO: 152) at the 3′ end.When the two strands are hybridised the fluorescence from thefluorescein is quenched by the local BHQ-1, and the substrate isessentially non-fluorescent. 1 μM of a capture strand (SEQ ID NO: 153)that is part-complementary to the lower strand of the fluorescentsubstrate is included in the assay. As shown in 2), in the presence ofATP (1 mM) and MgCl₂ (10 mM), appropriate helicase (10 nM) added to thesubstrate binds to the 3′ tail of the fluorescent substrate, moves alongthe upper strand, and displaces the complementary strand. As shown in3), once the complementary strand with BHQ-1 is fully displaced thefluorescein on the major strand fluoresces. As shown in 4) the displacedstrand preferentially anneals to an excess of capture strand to preventre-annealing of initial substrate and loss of fluorescence.

Results and Discussion

The graphs in FIGS. 16 and 17 show the dsDNA turnover (enzyme⁻¹min⁻¹) inbuffer (400 mM KCl, 100 mM Hepes pH 8.0, 1 mM ATP, 10 mM MgCl₂, 50 nMfluorescent substrate DNA (SEQ ID NOs: 151 and 152), 1 μM capture DNA(SEQ ID NO: 153)) for a number of helicases (Hel308 Mbu (labelled 1 inFIGS. 16 and 17, SEQ ID NO: 10), Hel308 Mbu-E284C (labelled 2 in FIGS.16 and 17, SEQ ID NO: 10 with the mutation E284C), Hel308Mbu-E284C/C301A (labelled 3 in FIG. 16, SEQ ID NO: 10 with the mutationsE284C/C301A), Hel308 Mbu-E285C (labelled 4 in FIG. 16, SEQ ID NO: 10with the mutation E285C), Hel308 Mbu-S288C (labelled 5 in FIG. 16, SEQID NO: 10 with the mutation S288C) and Hel308 Mbu-D274C (labelled 6 inFIG. 17, SEQ ID NO: 10 with the mutation D274C)). At the saltconcentration investigated (400 mM KCl) the following helicases Hel308Mbu-E284C (FIGS. 16 and 17 labelled 2, SEQ ID NO: 10 with the mutationE284C), Hel308 Mbu-E284C/C301 A (FIG. 16 labelled 3, SEQ ID NO: 10 withthe mutations E284C/C301A), Hel308 Mbu-E285C (FIG. 16 labelled 4, SEQ IDNO: 10 with the mutation E285C), Hel308 Mbu-S288C (FIG. 16 labelled 5,SEQ ID NO: 10 with the mutation S288C) and Hel308 Mbu-D274C (FIG. 17labelled 6, SEQ ID NO: 10 with the mutation D274C) exhibited a higherrate of dsDNA turnover than the control Hel308 Mbu (FIGS. 16 and 17labelled 1, SEQ ID NO: 10) (see FIGS. 16 and 17). This indicates thatthese enzymes show increased rate of turnover of dsDNA molecules(min⁻¹enzyme⁻¹) when compared to the Hel 308 Mbu control (SEQ ID NO: 10)under the conditions investigated.

Example 8

This example describes two procedures for the light treatment of Hel308Mbu-E284Faz (SEQ ID NO: 10 with the mutation E284Faz) and Hel308Mbu-S288Faz (SEQ ID NO: 10 with the mutation S288Faz).

Procedure 1—Exposure to UV Light

Hel308 Mbu-E284Faz (SEQ ID NO: 10 with the mutation E284Faz) or Hel308Mbu-S288Faz (SEQ ID NO: 10 with the mutation E288Faz) in storage buffer(50 mM Tris pH8.0 at 4° C., NaCl (360-390 mM) and 5% Glycerol) waspipetted into PCR tubes (Fisher 0.2 mL thin wall tubes). The sample wasplaced on ice and exposed to high intensity UV light at 254 nm(Spectroline Longlife Filter lamp (254 nm and 365 nm) from above, at adistance of 4.5 cm. The Hel308 Mbu-E284Faz (SEQ ID NO: 10 with themutation E284Faz) sample was exposed for 15 mins and the Hel308Mbu-S288Faz (SEQ ID NO: 10 with the mutation E288Faz) sample was exposedfor 10 mins. The samples were then both centrifuged for 5 mins at 16 000g to remove any precipitated protein. The soluble fraction was carefullyremoved from the insoluble pellet by pipette.

Procedure 2—Exposure to White Light (LED Source)

Hel308 Mbu-S288Faz (SEQ ID NO: 10 with the mutation E288Faz) in storagebuffer (50 mM Tris pH8.0 at 4° C., NaCl (370 mM) and 5% Glycerol) waspipetted into Microcentrifuge tube (Eppendorf, 1.5 mL, Protein Lo Bind).The sample was placed on ice (with the cap open) and exposed to LEDlight source (Schott A20960.1) on full power from above, at a distanceof 3 cm. The Hel308 Mbu-S288Faz (SEQ ID NO: 10 with the mutationE288Faz) sample was exposed for 3 hours.

Procedure 3—Exposure to White Light (LED Source) and Heating

Hel308 Mbu-S288Faz (SEQ ID NO: 10 with the mutation E288Faz) in storagebuffer (50 mM Tris pH8.0 at 4° C., NaCl (370 mM) and 5% Glycerol) waspipetted into Microcentrifuge tube (Eppendorf, 1.5 mL, Protein Lo Bind).The sample was placed on ice (with the cap open) and exposed to LEDlight source (Schott A20960.1) on full power from above, at a distanceof 1 cm. The Hel308 Mbu-S288Faz (SEQ ID NO: 10 with the mutationE288Faz) sample was exposed for 1 hour. The sample was transferred in aPCR tube (Fisher 0.2 mL thin wall tube) and heated at 50° C. for 10 minbefore ramping to 4° C., then centrifuged for 5 mins at 16 000 g toremove any precipitated protein. The soluble fraction was carefullyremoved from the insoluble pellet by pipette.

Example 9

This example compares the ability of Hel308 Mbu (SEQ ID NO: 10), tocontrol the movement of intact DNA strands (3.6 kb) through a nanopore,to that of a number of Hel308 Mbu mutants (Hel308 Mbu-E284C (SEQ ID NO:10 with the mutation E284C), Hel308 Mbu-S288C (SEQ ID NO: 10 with themutation S288C), Hel308 Mbu-E284Faz (SEQ ID NO: 10 with the mutationE284Faz) and heat treated Hel308 Mbu-E284Faz (SEQ ID NO: 10 with themutation E284Faz, the enzyme was heated in 50 mM Tris pH 8.0, 375 mMNaCl, 5% Glycerol buffer from 4° C. to 50° C. for 10 mins and thencooled to 4° C. in a BioRad PCR block)). The general method forcontrolled DNA translocation against the field is shown in FIG. 18.

Materials and Methods

Prior to setting up the experiment, the DNA (0.2 nM, (SEQ ID NO: 154attached at its 5′ end to four nitroindoles (labelled as x's in FIG.18), the last of which is attached to the 3′ end of SEQ ID NO: 155), SEQID NO: 156 and SEQ ID NO: 117) and appropriate helicase (Hel 308 Mbu(100 nM, SEQ ID NO: 10), Hel308 Mbu-E284C (100 nM, SEQ ID NO: 10 withthe mutation E284C), Hel308 Mbu-S288C (100 nM, SEQ ID NO: 10 with themutation S288C), Hel308 Mbu-E284Faz (100 nM, SEQ ID NO: 10 with themutation E284Faz) and heat treated Hel308 Mbu-E284Faz (500 nM, SEQ IDNO: 10 with the mutation E284Faz, the enzyme was heated in 50 mM Tris pH8.0, 375 mM NaCl, 5% Glycerol buffer from 4° C. to 50° C. for 10 minsand then cooled to 4° C. in a BioRad PCR block)) were dissolved inbuffer (960 mM KCl, 25 mM potassium phosphate, 3 mM potassiumferrocyanide, 1 mM potassium ferricyanide pH 8.0, 10 mM MgCl₂ and 1 mMATP).

Electrical measurements were acquired from single MspA nanopores(MS(B1-G75S/G77S/L88N/Q126R)8 MspA (SEQ ID NO: 2 with mutationsG75S/G77S/L88N/Q126R) inserted in block co-polymer in buffer (960 mMKCl, 25 mM potassium phosphate, 3 mM potassium ferrocyanide, 1 mMpotassium ferricyanide pH 8.0). After achieving a single pore in theblock co-polymer, buffer (3 mL of 960 mM KCl, 25 mM potassium phosphate,3 mM potassium ferrocyanide, 1 mM potassium ferricyanide pH 8.0) wasthen flowed through the system. Finally, the pre-mix (described above)was added to the single nanopore experimental system. Experiments werecarried out at a constant potential of +120 mV and helicase-controlledDNA movement was monitored.

Results and Discussion

Helicase controlled DNA movement was observed for all of the enzymestested—Hel 308 Mbu (SEQ ID NO: 10), Hel308 Mbu-E284C (SEQ ID NO: 10 withthe mutation E284C), Hel308 Mbu-S288C (SEQ ID NO: 10 with the mutationS288C), Hel308 Mbu-E284Faz (SEQ ID NO: 10 with the mutation E284Faz) andheat treated Hel308 Mbu-E284Faz (SEQ ID NO: 10 with the mutationE284Faz, the enzyme was heated in 50 mM Tris pH 8.0, 375 mM NaCl, 5%Glycerol buffer from 4° C. to 50° C. for 10 mins and then cooled to 4°C. in a BioRad PCR block). Example current traces showing helicasecontrolled DNA movement are shown in FIGS. 19-23. However, the mutantHel308 Mbu helicases (Hel308 Mbu-E284C (SEQ ID NO: 10 with the mutationE284C), Hel308 Mbu-S288C (SEQ ID NO: 10 with the mutation S288C), Hel308Mbu-E284Faz (SEQ ID NO: 10 with the mutation E284Faz) and heat treatedHel308 Mbu-E284Faz (SEQ ID NO: 10 with the mutation E284Faz, the enzymewas heated in 50 mM Tris pH 8.0, 375 mM NaCl, 5% Glycerol buffer from 4°C. to 50° C. for 10 mins and then cooled to 4° C. in a BioRad PCRblock)) showed increased processivity in comparison to Hel308 Mbu (SEQID NO: 10) see Table 11. Of the helicase controlled DNA movementsobserved in the experiments, the % of movements which processed the DNAall the way to the end of the strand (to the polyT region) weresignificantly higher for the mutant helicases (Hel3081Mbu-E284C (SEQ IDNO: 10 with the mutation E284C), Hel308 Mbu-S288C (SEQ ID NO: 10 withthe mutation S288C), Hel308 Mbu-E284Faz (SEQ ID NO: 10 with the mutationE284Faz) and heat treated Hel308 Mbu-E284Faz (SEQ ID NO: 10 with themutation E284Faz, the enzyme was heated in 50 mM Tris pH 8.0, 375 mMNaCl, 5% Glycerol buffer from 4° C. to 50° C. for 10 mins and thencooled to 4° C. in a BioRad PCR block)) when compared to Hel308 Mbu (SEQID NO: 10).

TABLE 11 % of Helicase Controlled DNA movement that reached the polyTregion of the DNA strand (SEQ ID NO: 154 attached at its 5′ end to fournitroindoles the last of which is attached to the Helicase 3′ end of SEQID NO:155) Hel308 Mbu (SEQ ID NO: 2 10) Hel308 Mbu-E284C (SEQ 32 ID NO:10 with the mutation E284C) Hel308 Mbu-E288C (SEQ 49 ID NO: 10 with themutation E288C) Hel308 Mbu-E284Faz (SEQ 28 ID NO: 10 with the mutationE284Faz) Heat treated Hel308 Mbu- 71 E284Faz (SEQ ID NO: 10 with themutation E284Faz, the enzyme was heated in 50 mM Tris pH 8.0, 375 mMNaCl, 5% Glycerol buffer from 4° C. to 50° C. for 10 mins and thencooled to 4° C. in a BioRad PCR block)

1.-59. (canceled)
 60. An NS3 helicase comprising a polynucleotidebinding domain which comprises in at least one conformational state anopening through which a polynucleotide can unbind from the helicase,wherein the helicase is modified such that two or more parts of thehelicase are connected using one or more linkers and wherein thehelicase retains its ability to control the movement of thepolynucleotide.
 61. An NS3 helicase according to claim 60, wherein thelinkers connect two amino acid residues that are located in differentstructural domains on the surface of the NS3 helicase surrounding thepolynucleotide binding domain.
 62. An NS3 helicase according to claim60, wherein the linkers connect two amino acid residues on one or moreloop regions connecting α-helices and β-strands of the NS3 helicaseand/or are spatially located proximal to the polynucleotide bindingdomain.
 63. An NS3 helicase according to claim 60, wherein the linkersconnect two amino acid residues that are located in different structuraldomains on the surface of the NS3 helicase surrounding thepolynucleotide binding domain or wherein the linkers connect two aminoacid residues on one or more loop regions connecting α-helices andβ-strands of the NS3 helicase and wherein at least one amino acid of thetwo amino acid residues is substituted with cysteine, a non-naturalamino acid or 4-azido-L-phenylalanine (Faz).
 64. An NS3 helicaseaccording to claim 60, wherein the one or more linkers are amino acidsequences and/or one or more chemical crosslinkers.
 65. An NS3 helicaseaccording to claim 60, wherein the linkers comprise a polyethyleneglycol(PEG), polysaccharide, or polyamide.
 66. An NS3 helicase according toclaim 60, wherein the linkers comprise a deoxyribonucleic acid (DNA)sequence, peptide nucleic acid (PNA), threose nucleic acid (TNA), orglycerol nucleic acid (GNA).
 67. An NS3 helicase according to claim 60,wherein one end or both ends of the one or more linkers are covalentlyattached to the helicase.
 68. An NS3 helicase according to claim 60,wherein the helicase has a covalently closed structure.
 69. An NS3helicase according to claim 60, wherein the helicase further comprises asecond set of two amino acid residues in different structural domains ofthe helicase surrounding the polynucleotide binding domain that areartificially covalently connected via a linkage between the two aminoacid residues of the second set.
 70. A complex comprising (i) an NS3helicase that comprises a polynucleotide binding domain and (ii) atarget polynucleotide bound to the polynucleotide binding domain,wherein two amino acid residues that are located in different structuraldomains on the surface of the NS3 helicase surrounding thepolynucleotide binding domain are artificially covalently connected viaa linkage between the two amino acid residues, such that the helicasehas a covalently-closed structure.
 71. A complex according to claim 70,wherein the distance between the two amino acids is less than 50Angstroms (Å), wherein the bound target polynucleotide is encircled bythe covalently-closed structure.